HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229431821G>T , CM000663.2:g.229431821G>T | GRCh38 |
NC_000001.10:g.229567568G>T , CM000663.1:g.229567568G>T | GRCh37 |
NC_000001.9:g.227634191G>T | NCBI36 |
NG_006672.1:g.7276C>A , LRG_429:g.7276C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.890C>A | ENSP00000355644.4:p.Ala297Asp | |
ENST00000684723.1:c.755C>A | ENSP00000508084.1:p.Ala252Asp | |
ENST00000366683.3:c.521C>A | ENSP00000355644.3:p.Ala174Asp | |
ENST00000366684.7:c.890C>A MANE Select | ENSP00000355645.3:p.Ala297Asp | |
NM_001100.3:c.890C>A , LRG_429t1:c.890C>A | NP_001091.1:p.Ala297Asp | |
NM_001100.4:c.890C>A MANE Select | NP_001091.1:p.Ala297Asp |