Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.112832715C>A , CM000664.2:g.112832715C>A | GRCh38 |
| NC_000002.11:g.113590292C>A , CM000664.1:g.113590292C>A | GRCh37 |
| NC_000002.10:g.113306763C>A | NCBI36 |
| NG_008851.1:g.9065G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263341.7:c.413G>T MANE Select | ENSP00000263341.2:p.Gly138Val | |
| ENST00000263341.6:c.413G>T | ENSP00000263341.2:p.Gly138Val | |
| ENST00000418817.5:c.413G>T | ENSP00000407219.1:p.Gly138Val | |
| ENST00000487639.1:n.314G>T | ||
| ENST00000491056.5:n.1220G>T | ||
| NM_000576.2:c.413G>T | NP_000567.1:p.Gly138Val | |
| XM_006712496.1:c.179G>T | XP_006712559.1:p.Gly60Val | |
| XM_017003988.2:c.320G>T | XP_016859477.1:p.Gly107Val | |
| NM_000576.3:c.413G>T MANE Select | NP_000567.1:p.Gly138Val |