Linked Data
dbSNP Id:
rs2145904163
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18789282A>T , CM000681.2:g.18789282A>T | GRCh38 |
| NC_000019.9:g.18900091A>T , CM000681.1:g.18900091A>T | GRCh37 |
| NC_000019.8:g.18761091A>T | NCBI36 |
| NG_007070.1:g.7024T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.406T>A MANE Select | ENSP00000222271.2:p.Cys136Ser | |
| ENST00000222271.6:c.406T>A | ENSP00000222271.2:p.Cys136Ser | |
| ENST00000425807.1:c.391-390T>A | ENSP00000403792.1:n.391-390T>A | |
| ENST00000542601.6:c.307T>A | ENSP00000439156.2:p.Cys103Ser | |
| NM_000095.2:c.406T>A | NP_000086.2:p.Cys136Ser | |
| NM_000095.3:c.406T>A MANE Select | NP_000086.2:p.Cys136Ser |