Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144252T>G , CM000670.2:g.38144252T>G | GRCh38 |
| NC_000008.10:g.38001770T>G , CM000670.1:g.38001770T>G | GRCh37 |
| NC_000008.9:g.38120927T>G | NCBI36 |
| NG_011827.1:g.11831A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.*21A>C MANE Select | ENSP00000276449.3:n.*21A>C | |
| ENST00000276449.8:c.*21A>C | ENSP00000276449.3:n.*21A>C | |
| ENST00000520114.1:n.2848A>C | ||
| ENST00000522050.1:c.721A>C | ||
| NM_000349.2:c.*21A>C | NP_000340.2:n.*21A>C | |
| XM_006716392.1:c.785A>C | XP_006716455.1:p.Asn262Thr | |
| NM_000349.3:c.*21A>C MANE Select | NP_000340.2:n.*21A>C |