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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.119033121C>A , CM000663.2:g.119033121C>A
GRCh38
NC_000001.10:g.119575744C>A , CM000663.1:g.119575744C>A
GRCh37
NC_000001.9:g.119377267C>A
NCBI36
NG_050658.1:g.112668G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000235521.5:c.873G>T
MANE Select
ENSP00000235521.4:p.Val291=
ENST00000235521.4:c.873G>T
ENSP00000235521.4:p.Val291=
ENST00000369426.9:c.*239G>T
ENSP00000358434.5:n.*239G>T
NM_015836.3:c.873G>T
NP_056651.1:p.Val291=
NM_201263.2:c.*239G>T
NP_957715.1:n.*239G>T
XM_005270350.2:c.819G>T
XP_005270407.1:p.Val273=
XM_006710283.1:c.591G>T
XP_006710346.1:p.Val197=
XM_011540493.1:c.804G>T
XP_011538795.1:p.Val268=
XM_011540494.1:c.804G>T
XP_011538796.1:p.Val268=
XM_011540495.1:c.615G>T
XP_011538797.1:p.Val205=
XM_005270350.3:c.819G>T
XP_005270407.1:p.Val273=
XM_011540494.2:c.804G>T
XP_011538796.1:p.Val268=
XM_011540495.2:c.615G>T
XP_011538797.1:p.Val205=
XM_017000038.1:c.816G>T
XP_016855527.1:p.Val272=
XM_017000039.1:c.804G>T
XP_016855528.1:p.Val268=
XM_017000040.1:c.702G>T
XP_016855529.1:p.Val234=
XM_017000041.2:c.534G>T
XP_016855530.1:p.Val178=
XM_017000042.1:c.*208G>T
XP_016855531.1:n.*208G>T
XM_024449826.1:c.804G>T
XP_024305594.1:p.Val268=
XM_024449860.1:c.591G>T
XP_024305628.1:p.Val197=
XM_024449871.1:c.591G>T
XP_024305639.1:p.Val197=
NM_001378226.1:c.804G>T
NP_001365155.1:p.Val268=
NM_001378227.1:c.804G>T
NP_001365156.1:p.Val268=
NM_001378228.1:c.702G>T
NP_001365157.1:p.Val234=
NM_001378229.1:c.615G>T
NP_001365158.1:p.Val205=
NM_001378230.1:c.591G>T
NP_001365159.1:p.Val197=
NM_001378231.1:c.*208G>T
NP_001365160.1:n.*208G>T
NM_015836.4:c.873G>T
MANE Select
NP_056651.1:p.Val291=