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Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.141647431C= , CM000667.2:g.141647431C=
GRCh38
NC_000005.9:g.141026998C= , CM000667.1:g.141026998C=
GRCh37
NC_000005.8:g.141007182C=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000435817.7:c.795G=
MANE Select
ENSP00000399259.2:p.Glu265=
ENST00000435817.6:c.795G=
ENSP00000399259.2:p.Glu265=
ENST00000522126.5:c.567G=
ENSP00000427796.1:p.Glu189=
ENST00000522386.1:n.401G=
ENST00000522763.5:n.99G=
ENST00000522783.5:c.789G=
ENSP00000428677.1:p.Glu263=
ENST00000523856.5:n.53G=
NM_033449.2:c.795G=
NP_258260.1:p.Glu265=
XM_005268524.3:c.789G=
XP_005268581.1:p.Glu263=
XM_006714803.2:c.666G=
XP_006714866.1:p.Glu222=
XM_011537698.1:c.795G=
XP_011536000.1:p.Glu265=
XM_011537699.1:c.795G=
XP_011536001.1:p.Glu265=
XM_011537700.1:c.795G=
XP_011536002.1:p.Glu265=
XM_011537701.1:c.795G=
XP_011536003.1:p.Glu265=
XR_427781.2:n.849G=
XR_944338.1:n.855G=
XR_944339.1:n.855G=
XM_005268524.5:c.789G=
XP_005268581.1:p.Glu263=
XM_006714803.4:c.666G=
XP_006714866.1:p.Glu222=
XM_011537698.3:c.795G=
XP_011536000.1:p.Glu265=
XM_011537700.3:c.795G=
XP_011536002.1:p.Glu265=
XM_011537701.3:c.795G=
XP_011536003.1:p.Glu265=
XM_017010013.2:c.795G=
XP_016865502.1:p.Glu265=
XR_002956197.1:n.791G=
XR_427781.4:n.791G=
XR_944338.3:n.870G=
XR_944339.3:n.870G=
NM_033449.3:c.795G=
MANE Select
NP_258260.1:p.Glu265=