HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320501C>T , CM000667.2:g.159320501C>T | GRCh38 |
NC_000005.9:g.158747509C>T , CM000667.1:g.158747509C>T | GRCh37 |
NC_000005.8:g.158680087C>T | NCBI36 |
NG_009618.1:g.14973G>A , LRG_71:g.14973G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.-129G>A | ENSP00000512849.1:n.-129G>A | |
ENST00000696751.1:c.384G>A | ENSP00000512850.1:p.Gly128= | |
ENST00000231228.3:c.502G>A MANE Select | ENSP00000231228.2:p.Val168Met | |
ENST00000231228.2:c.502G>A | ENSP00000231228.2:p.Val168Met | |
NM_002187.2:c.502G>A , LRG_71t1:c.502G>A | NP_002178.2:p.Val168Met | |
XR_001742945.1:n.52C>T | ||
NM_002187.3:c.502G>A MANE Select | NP_002178.2:p.Val168Met |