HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3154574G>T , CM000668.2:g.3154574G>T | GRCh38 |
NC_000006.11:g.3154808G>T , CM000668.1:g.3154808G>T | GRCh37 |
NC_000006.10:g.3099807G>T | NCBI36 |
NG_042223.1:g.7976C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333628.4:c.627C>A MANE Select | ENSP00000369703.2:p.Asp209Glu | |
ENST00000679400.1:n.683C>A | ||
ENST00000679907.1:n.1015C>A | ||
ENST00000680036.1:n.1409C>A | ||
ENST00000680967.1:n.1717C>A | ||
ENST00000333628.3:c.627C>A | ENSP00000369703.2:p.Asp209Glu | |
NM_001069.2:c.627C>A | NP_001060.1:p.Asp209Glu | |
NM_001310315.1:c.372C>A | NP_001297244.1:p.Asp124Glu | |
NM_001069.3:c.627C>A MANE Select | NP_001060.1:p.Asp209Glu | |
NM_001310315.2:c.372C>A | NP_001297244.1:p.Asp124Glu |