Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119677053A>T , CM000672.2:g.119677053A>T | GRCh38 |
| NC_000010.10:g.121436565A>T , CM000672.1:g.121436565A>T | GRCh37 |
| NC_000010.9:g.121426555A>T | NCBI36 |
| NG_016125.1:g.30684A>T , LRG_742:g.30684A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.1499A>T MANE Select | ENSP00000358081.4:p.Asp500Val | |
| ENST00000369085.7:c.1499A>T | ENSP00000358081.3:p.Asp500Val | |
| NM_004281.3:c.1499A>T , LRG_742t1:c.1499A>T | NP_004272.2:p.Asp500Val | |
| XM_005270287.1:c.1496A>T | XP_005270344.1:p.Asp499Val | |
| XM_005270287.2:c.1496A>T | XP_005270344.1:p.Asp499Val | |
| NM_004281.4:c.1499A>T MANE Select | NP_004272.2:p.Asp500Val |