HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432170A>T , CM000663.2:g.229432170A>T | GRCh38 |
NC_000001.10:g.229567917A>T , CM000663.1:g.229567917A>T | GRCh37 |
NC_000001.9:g.227634540A>T | NCBI36 |
NG_006672.1:g.6927T>A , LRG_429:g.6927T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366683.4:c.632T>A | ENSP00000355644.4:p.Val211Glu | |
ENST00000684723.1:c.497T>A | ENSP00000508084.1:p.Val166Glu | |
ENST00000366683.3:c.479+237T>A | ENSP00000355644.3:n.479+237T>A | |
ENST00000366684.7:c.632T>A MANE Select | ENSP00000355645.3:p.Val211Glu | |
NM_001100.3:c.632T>A , LRG_429t1:c.632T>A | NP_001091.1:p.Val211Glu | |
NM_001100.4:c.632T>A MANE Select | NP_001091.1:p.Val211Glu |