Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109264386T>A , CM000663.2:g.109264386T>A | GRCh38 |
| NC_000001.10:g.109807008T>A , CM000663.1:g.109807008T>A | GRCh37 |
| NC_000001.9:g.109608531T>A | NCBI36 |
| NG_052669.1:g.19682T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271332.4:c.5289+21T>A MANE Select | ENSP00000271332.3:n.5289+21T>A | |
| ENST00000271332.3:c.5289+21T>A | ENSP00000271332.3:n.5289+21T>A | |
| NM_001408.2:c.5289+21T>A | NP_001399.1:n.5289+21T>A | |
| XM_005270580.3:c.5289+21T>A | XP_005270637.1:n.5289+21T>A | |
| NM_001408.3:c.5289+21T>A MANE Select | NP_001399.1:n.5289+21T>A |