This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20187927C>G , CM000675.2:g.20187927C>G | GRCh38 |
| NC_000013.10:g.20762066C>G , CM000675.1:g.20762066C>G | GRCh37 |
| NC_000013.9:g.19660066C>G | NCBI36 |
| NG_008358.1:g.10049G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.*974G>C | ENSP00000372295.1:n.*974G>C | |
| ENST00000382848.5:c.*974G>C MANE Select | ENSP00000372299.4:n.*974G>C | |
| ENST00000382844.1:c.*974G>C | ENSP00000372295.1:n.*974G>C | |
| ENST00000382848.4:c.*974G>C | ENSP00000372299.4:n.*974G>C | |
| NM_004004.5:c.*974G>C | NP_003995.2:n.*974G>C | |
| XM_011535049.1:c.*974G>C | XP_011533351.1:n.*974G>C | |
| XM_011535049.2:c.*974G>C | XP_011533351.1:n.*974G>C | |
| NM_004004.6:c.*974G>C MANE Select | NP_003995.2:n.*974G>C |