Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24799822G>A , CM000666.2:g.24799822G>A | GRCh38 |
| NC_000004.11:g.24801444G>A , CM000666.1:g.24801444G>A | GRCh37 |
| NC_000004.10:g.24410542G>A | NCBI36 |
| NG_012213.1:g.9360G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.301G>A MANE Select | ENSP00000371554.3:p.Gly101Ser | |
| ENST00000382120.3:c.301G>A | ENSP00000371554.3:p.Gly101Ser | |
| NM_003102.2:c.301G>A | NP_003093.2:p.Gly101Ser | |
| XR_427488.1:n.491G>A | ||
| NM_003102.3:c.301G>A | NP_003093.2:p.Gly101Ser | |
| NM_003102.4:c.301G>A MANE Select | NP_003093.2:p.Gly101Ser |