Linked Data
dbSNP Id:
rs1208032174
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928876C>A , CM000684.2:g.43928876C>A | GRCh38 |
| NC_000022.10:g.44324756C>A , CM000684.1:g.44324756C>A | GRCh37 |
| NC_000022.9:g.42656089C>A | NCBI36 |
| NG_008631.1:g.10138C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.473C>A MANE Select | ENSP00000216180.3:p.Ser158Tyr | |
| ENST00000216180.7:c.473C>A | ENSP00000216180.3:p.Ser158Tyr | |
| ENST00000406117.6:c.*105C>A | ENSP00000384668.2:n.*105C>A | |
| ENST00000423180.2:c.461C>A | ENSP00000397987.2:p.Ser154Tyr | |
| ENST00000478713.1:n.507C>A | ||
| NM_025225.2:c.473C>A | NP_079501.2:p.Ser158Tyr | |
| NM_025225.3:c.473C>A MANE Select | NP_079501.2:p.Ser158Tyr |