HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41624129G>A , CM000679.2:g.41624129G>A | GRCh38 |
NC_000017.10:g.39780381G>A , CM000679.1:g.39780381G>A | GRCh37 |
NC_000017.9:g.37033907G>A | NCBI36 |
NG_008625.1:g.5502C>T | |
NG_009090.2:g.167584C>T , LRG_401:g.167584C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000311208.13:c.381C>T MANE Select | ENSP00000308452.8:p.Pro127= | |
ENST00000311208.12:c.381C>T | ENSP00000308452.8:p.Pro127= | |
ENST00000463128.5:c.-235C>T | ENSP00000468672.1:n.-235C>T | |
ENST00000491673.1:n.447C>T | ||
ENST00000493253.5:n.168C>T | ||
ENST00000540235.5:c.132C>T | ENSP00000441751.2:p.Pro44= | |
ENST00000577817.3:c.336C>T | ENSP00000467418.1:p.Pro112= | |
NM_000422.2:c.381C>T | NP_000413.1:p.Pro127= | |
NM_000422.3:c.381C>T MANE Select | NP_000413.1:p.Pro127= |