Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571602C>A , CM000663.2:g.154571602C>A | GRCh38 |
| NC_000001.10:g.154544078C>A , CM000663.1:g.154544078C>A | GRCh37 |
| NC_000001.9:g.152810702C>A | NCBI36 |
| NG_008027.1:g.8822C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.779C>A MANE Select | ENSP00000357461.3:p.Ser260Tyr | |
| ENST00000636034.1:c.779C>A | ENSP00000489703.1:p.Ser260Tyr | |
| ENST00000637900.1:c.785C>A | ENSP00000490474.1:p.Ser262Tyr | |
| ENST00000368476.3:c.779C>A | ENSP00000357461.3:p.Ser260Tyr | |
| NM_000748.2:c.779C>A | NP_000739.1:p.Ser260Tyr | |
| XM_017000180.2:c.269C>A | XP_016855669.1:p.Ser90Tyr | |
| XR_001736952.2:n.1031C>A | ||
| NM_000748.3:c.779C>A MANE Select | NP_000739.1:p.Ser260Tyr |