Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665984T>A , CM000679.2:g.39665984T>A | GRCh38 |
| NC_000017.10:g.37822237T>A , CM000679.1:g.37822237T>A | GRCh37 |
| NC_000017.9:g.35075763T>A | NCBI36 |
| NG_008892.1:g.5639T>A , LRG_210:g.5639T>A | |
| NG_042278.1:g.3004T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.379T>A MANE Select | ENSP00000312624.2:p.Cys127Ser | |
| ENST00000309889.2:c.379T>A | ENSP00000312624.2:p.Cys127Ser | |
| ENST00000578283.1:c.307T>A | ENSP00000462787.1:p.Cys103Ser | |
| NM_003673.3:c.379T>A , LRG_210t1:c.379T>A | NP_003664.1:p.Cys127Ser | |
| NM_003673.4:c.379T>A MANE Select | NP_003664.1:p.Cys127Ser |