Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38687939G>T , CM000675.2:g.38687939G>T | GRCh38 |
| NC_000013.10:g.39262076G>T , CM000675.1:g.39262076G>T | GRCh37 |
| NC_000013.9:g.38160076G>T | NCBI36 |
| NG_008125.2:g.5904G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.595G>T MANE Select | NP_997244.4:p.Ala199Ser |
| ENST00000280481.9:c.595G>T MANE Select | ENSP00000280481.7:p.Ala199Ser |
| NM_207361.5:c.595G>T | NP_997244.4:p.Ala199Ser |
| ENST00000280481.8:c.595G>T | ENSP00000280481.7:p.Ala199Ser |
| XM_011535057.1:c.595G>T | XP_011533359.1:p.Ala199Ser |
| XM_017020554.1:c.595G>T | XP_016876043.1:p.Ala199Ser |
| XR_941571.1:n.903G>T | |
| XR_941571.2:n.899G>T |