HGVS | Genome Assembly |
---|---|
NC_000023.11:g.119930199T>C , CM000685.2:g.119930199T>C | GRCh38 |
NC_000023.10:g.119064162T>C , CM000685.1:g.119064162T>C | GRCh37 |
NC_000023.9:g.118948190T>C | NCBI36 |
NG_021260.1:g.18574A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371410.5:c.924-34A>G MANE Select | ENSP00000360464.3:n.924-34A>G | |
ENST00000652253.1:c.920-34A>G | ||
ENST00000371410.4:c.924-34A>G | ENSP00000360464.3:n.924-34A>G | |
ENST00000477789.5:n.1852-34A>G | ||
ENST00000482407.1:n.723-34A>G | ||
NM_024528.3:c.924-34A>G | NP_078804.2:n.924-34A>G | |
XM_017029842.1:c.627-34A>G | XP_016885331.1:n.627-34A>G | |
NM_024528.4:c.924-34A>G MANE Select | NP_078804.2:n.924-34A>G |