HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41623814A>G , CM000679.2:g.41623814A>G | GRCh38 |
NC_000017.10:g.39780066A>G , CM000679.1:g.39780066A>G | GRCh37 |
NC_000017.9:g.37033592A>G | NCBI36 |
NG_008625.1:g.5817T>C | |
NG_009090.2:g.167899T>C , LRG_401:g.167899T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311208.13:c.432+264T>C MANE Select | ENSP00000308452.8:n.432+264T>C | |
ENST00000311208.12:c.432+264T>C | ENSP00000308452.8:n.432+264T>C | |
ENST00000463128.5:c.-184+264T>C | ENSP00000468672.1:n.-184+264T>C | |
ENST00000491673.1:n.498+264T>C | ||
ENST00000493253.5:n.219+264T>C | ||
ENST00000540235.5:c.183+264T>C | ENSP00000441751.2:n.183+264T>C | |
ENST00000577817.3:c.387+264T>C | ENSP00000467418.1:n.387+264T>C | |
NM_000422.2:c.432+264T>C | NP_000413.1:n.432+264T>C | |
NM_000422.3:c.432+264T>C MANE Select | NP_000413.1:n.432+264T>C |