Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94021692G>T , CM000663.2:g.94021692G>T | GRCh38 |
| NC_000001.10:g.94487248G>T , CM000663.1:g.94487248G>T | GRCh37 |
| NC_000001.9:g.94259836G>T | NCBI36 |
| NG_009073.1:g.104458C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4796C>A MANE Select | ENSP00000359245.3:p.Ser1599Tyr | |
| ENST00000370225.3:c.4796C>A | ENSP00000359245.3:p.Ser1599Tyr | |
| ENST00000460514.1:n.290C>A | ||
| ENST00000536513.5:c.1172C>A | ENSP00000439707.2:p.Ser391Tyr | |
| NM_000350.2:c.4796C>A | NP_000341.2:p.Ser1599Tyr | |
| NM_000350.3:c.4796C>A MANE Select | NP_000341.2:p.Ser1599Tyr |