Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38691105T>A , CM000675.2:g.38691105T>A | GRCh38 |
| NC_000013.10:g.39265242T>A , CM000675.1:g.39265242T>A | GRCh37 |
| NC_000013.9:g.38163242T>A | NCBI36 |
| NG_008125.2:g.9070T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.3761T>A MANE Select | NP_997244.4:p.Leu1254Ter |
| ENST00000280481.9:c.3761T>A MANE Select | ENSP00000280481.7:p.Leu1254Ter |
| NM_207361.5:c.3761T>A | NP_997244.4:p.Leu1254Ter |
| ENST00000280481.8:c.3761T>A | ENSP00000280481.7:p.Leu1254Ter |
| XM_011535057.1:c.3761T>A | XP_011533359.1:p.Leu1254Ter |
| XM_017020554.1:c.3761T>A | XP_016876043.1:p.Leu1254Ter |
| XR_941571.1:n.4069T>A | |
| XR_941571.2:n.4065T>A |