Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.21845311C>A , CM000685.2:g.21845311C>A | GRCh38 |
| NC_000023.10:g.21863429C>A , CM000685.1:g.21863429C>A | GRCh37 |
| NC_000023.9:g.21773350C>A | NCBI36 |
| NG_012797.1:g.10774C>A | |
| NG_012797.2:g.10774C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379484.10:c.365C>A MANE Select | ENSP00000368798.5:p.Ser122Tyr | |
| ENST00000365779.2:c.365C>A | ENSP00000368796.1:p.Ser122Tyr | |
| ENST00000379484.9:c.365C>A | ENSP00000368798.5:p.Ser122Tyr | |
| ENST00000465888.1:n.464C>A | ||
| NM_015884.3:c.365C>A | NP_056968.1:p.Ser122Tyr | |
| NM_015884.4:c.365C>A MANE Select | NP_056968.1:p.Ser122Tyr |