HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41624352C>A , CM000679.2:g.41624352C>A | GRCh38 |
NC_000017.10:g.39780604C>A , CM000679.1:g.39780604C>A | GRCh37 |
NC_000017.9:g.37034130C>A | NCBI36 |
NG_008625.1:g.5279G>T | |
NG_009090.2:g.167361G>T , LRG_401:g.167361G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311208.13:c.158G>T MANE Select | ENSP00000308452.8:p.Gly53Val | |
ENST00000311208.12:c.158G>T | ENSP00000308452.8:p.Gly53Val | |
ENST00000463128.5:c.-312-146G>T | ENSP00000468672.1:n.-312-146G>T | |
ENST00000491673.1:n.224G>T | ||
ENST00000540235.5:c.-48G>T | ENSP00000441751.2:n.-48G>T | |
ENST00000577817.3:c.113G>T | ENSP00000467418.1:p.Gly38Val | |
NM_000422.2:c.158G>T | NP_000413.1:p.Gly53Val | |
NM_000422.3:c.158G>T MANE Select | NP_000413.1:p.Gly53Val |