Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.255882A>C , CM000669.2:g.255882A>C | GRCh38 |
| NC_000007.13:g.295848A>C , CM000669.1:g.295848A>C | GRCh37 |
| NG_033970.1:g.65518A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313766.6:c.1106A>C MANE Select | ENSP00000322323.5:p.Tyr369Ser | |
| ENST00000313766.5:c.1106A>C | ENSP00000322323.5:p.Tyr369Ser | |
| ENST00000515795.1:n.763A>C | ||
| NM_020223.3:c.1106A>C | NP_064608.2:p.Tyr369Ser | |
| XR_242097.3:n.1253A>C | ||
| XM_017012450.1:c.1367A>C | XP_016867939.1:p.Tyr456Ser | |
| XM_017012451.1:c.1364A>C | XP_016867940.1:p.Tyr455Ser | |
| XM_017012455.2:c.404A>C | XP_016867944.1:p.Tyr135Ser | |
| NM_020223.4:c.1106A>C MANE Select | NP_064608.2:p.Tyr369Ser |