Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.173019499A>T , CM000665.2:g.173019499A>T | GRCh38 |
| NC_000003.11:g.172737289A>T , CM000665.1:g.172737289A>T | GRCh37 |
| NC_000003.10:g.174219983A>T | NCBI36 |
| NG_021422.1:g.126770T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351008.4:c.835T>A MANE Select | ENSP00000341765.3:p.Ser279Thr | |
| ENST00000351008.3:c.835T>A | ENSP00000341765.3:p.Ser279Thr | |
| NM_031955.5:c.835T>A | NP_114161.3:p.Ser279Thr | |
| XM_006713778.2:c.835T>A | XP_006713841.1:p.Ser279Thr | |
| XM_011513222.1:c.835T>A | XP_011511524.1:p.Ser279Thr | |
| XM_006713778.3:c.835T>A | XP_006713841.1:p.Ser279Thr | |
| XM_017007308.2:c.835T>A | XP_016862797.1:p.Ser279Thr | |
| NM_031955.6:c.835T>A MANE Select | NP_114161.3:p.Ser279Thr |