HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41623776T>A , CM000679.2:g.41623776T>A | GRCh38 |
NC_000017.10:g.39780028T>A , CM000679.1:g.39780028T>A | GRCh37 |
NC_000017.9:g.37033554T>A | NCBI36 |
NG_008625.1:g.5855A>T | |
NG_009090.2:g.167937A>T , LRG_401:g.167937A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311208.13:c.432+302A>T MANE Select | ENSP00000308452.8:n.432+302A>T | |
ENST00000311208.12:c.432+302A>T | ENSP00000308452.8:n.432+302A>T | |
ENST00000463128.5:c.-184+302A>T | ENSP00000468672.1:n.-184+302A>T | |
ENST00000491673.1:n.498+302A>T | ||
ENST00000493253.5:n.219+302A>T | ||
ENST00000540235.5:c.183+302A>T | ENSP00000441751.2:n.183+302A>T | |
ENST00000577817.3:c.387+302A>T | ENSP00000467418.1:n.387+302A>T | |
NM_000422.2:c.432+302A>T | NP_000413.1:n.432+302A>T | |
NM_000422.3:c.432+302A>T MANE Select | NP_000413.1:n.432+302A>T |