HGVS | Genome Assembly |
---|---|
NC_000023.11:g.119930176A>T , CM000685.2:g.119930176A>T | GRCh38 |
NC_000023.10:g.119064139A>T , CM000685.1:g.119064139A>T | GRCh37 |
NC_000023.9:g.118948167A>T | NCBI36 |
NG_021260.1:g.18597T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371410.5:c.924-11T>A MANE Select | ENSP00000360464.3:n.924-11T>A | |
ENST00000652253.1:c.920-11T>A | ||
ENST00000371410.4:c.924-11T>A | ENSP00000360464.3:n.924-11T>A | |
ENST00000477789.5:n.1852-11T>A | ||
ENST00000482407.1:n.723-11T>A | ||
NM_024528.3:c.924-11T>A | NP_078804.2:n.924-11T>A | |
XM_017029842.1:c.627-11T>A | XP_016885331.1:n.627-11T>A | |
NM_024528.4:c.924-11T>A MANE Select | NP_078804.2:n.924-11T>A |