Linked Data
dbSNP Id:
rs2120109982
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69648120C>A , CM000673.2:g.69648120C>A | GRCh38 |
| NC_000011.9:g.69462888C>A , CM000673.1:g.69462888C>A | GRCh37 |
| NC_000011.8:g.69172069C>A | NCBI36 |
| NG_007375.1:g.12016C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.701C>A MANE Select | ENSP00000227507.2:p.Ser234Tyr | |
| ENST00000227507.2:c.701C>A | ENSP00000227507.2:p.Ser234Tyr | |
| ENST00000536559.1:c.*121C>A | ENSP00000438482.1:n.*121C>A | |
| ENST00000542367.1:n.164C>A | ||
| ENST00000545484.1:n.407C>A | ||
| NM_053056.2:c.701C>A | NP_444284.1:p.Ser234Tyr | |
| XM_006718653.2:c.725C>A | XP_006718716.1:p.Ser242Tyr | |
| NM_053056.3:c.701C>A MANE Select | NP_444284.1:p.Ser234Tyr |