HGVS | Genome Assembly |
---|---|
NC_000019.10:g.57248650G>A , CM000681.2:g.57248650G>A | GRCh38 |
NC_000019.9:g.57760018G>A , CM000681.1:g.57760018G>A | GRCh37 |
NC_000019.8:g.62451830G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000414468.3:c.203G>A MANE Select | ENSP00000412999.1:p.Gly68Glu | |
ENST00000354309.4:c.-197G>A | ENSP00000365414.2:n.-197G>A | |
ENST00000414468.2:c.203G>A | ENSP00000412999.1:p.Gly68Glu | |
NM_001023563.3:c.203G>A | NP_001018857.2:p.Gly68Glu | |
NM_001145078.1:c.-197G>A | NP_001138550.1:n.-197G>A | |
NM_001023563.4:c.203G>A MANE Select | NP_001018857.2:p.Gly68Glu | |
NM_001145078.2:c.-197G>A | NP_001138550.1:n.-197G>A |