Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80273845G>A , CM000672.2:g.80273845G>A | GRCh38 |
| NC_000010.10:g.82033601G>A , CM000672.1:g.82033601G>A | GRCh37 |
| NC_000010.9:g.82023581G>A | NCBI36 |
| NG_008083.1:g.20834C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.1124C>T MANE Select | ENSP00000361287.3:p.Ala375Val | |
| ENST00000372213.7:c.1124C>T | ENSP00000361287.3:p.Ala375Val | |
| ENST00000480845.1:n.356C>T | ||
| ENST00000485270.5:n.636C>T | ||
| NM_000429.2:c.1124C>T | NP_000420.1:p.Ala375Val | |
| XM_005269842.3:c.1124C>T | XP_005269899.1:p.Ala375Val | |
| XM_005269843.3:c.1001C>T | XP_005269900.1:p.Ala334Val | |
| NM_000429.3:c.1124C>T MANE Select | NP_000420.1:p.Ala375Val |