HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41623754C>A , CM000679.2:g.41623754C>A | GRCh38 |
NC_000017.10:g.39780006C>A , CM000679.1:g.39780006C>A | GRCh37 |
NC_000017.9:g.37033532C>A | NCBI36 |
NG_008625.1:g.5877G>T | |
NG_009090.2:g.167959G>T , LRG_401:g.167959G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311208.13:c.432+324G>T MANE Select | ENSP00000308452.8:n.432+324G>T | |
ENST00000311208.12:c.432+324G>T | ENSP00000308452.8:n.432+324G>T | |
ENST00000463128.5:c.-184+324G>T | ENSP00000468672.1:n.-184+324G>T | |
ENST00000491673.1:n.498+324G>T | ||
ENST00000493253.5:n.219+324G>T | ||
ENST00000540235.5:c.183+324G>T | ENSP00000441751.2:n.183+324G>T | |
ENST00000577817.3:c.387+324G>T | ENSP00000467418.1:n.387+324G>T | |
NM_000422.2:c.432+324G>T | NP_000413.1:n.432+324G>T | |
NM_000422.3:c.432+324G>T MANE Select | NP_000413.1:n.432+324G>T |