HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41624086G>A , CM000679.2:g.41624086G>A | GRCh38 |
NC_000017.10:g.39780338G>A , CM000679.1:g.39780338G>A | GRCh37 |
NC_000017.9:g.37033864G>A | NCBI36 |
NG_008625.1:g.5545C>T | |
NG_009090.2:g.167627C>T , LRG_401:g.167627C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311208.13:c.424C>T MANE Select | ENSP00000308452.8:p.Gln142Ter | |
ENST00000311208.12:c.424C>T | ENSP00000308452.8:p.Gln142Ter | |
ENST00000463128.5:c.-192C>T | ENSP00000468672.1:n.-192C>T | |
ENST00000491673.1:n.490C>T | ||
ENST00000493253.5:n.211C>T | ||
ENST00000540235.5:c.175C>T | ENSP00000441751.2:p.Gln59Ter | |
ENST00000577817.3:c.379C>T | ENSP00000467418.1:p.Gln127Ter | |
NM_000422.2:c.424C>T | NP_000413.1:p.Gln142Ter | |
NM_000422.3:c.424C>T MANE Select | NP_000413.1:p.Gln142Ter |