Canonical Allele Identifier: CA2034911848

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966214G= , CM000674.2:g.48966214G=	GRCh38
NC_000012.11:g.49359997G= , CM000674.1:g.49359997G=	GRCh37
NC_000012.10:g.47646264G=	NCBI36
NG_023347.1:g.10645C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000301061.9:c.1051C= MANE Select	ENSP00000301061.4:p.Arg351=
ENST00000301061.8:c.1051C=	ENSP00000301061.4:p.Arg351=
ENST00000403957.5:c.*333C=	ENSP00000385980.1:n.*333C=
ENST00000407467.5:c.*333C=	ENSP00000384691.1:n.*333C=
NM_003394.3:c.1051C=	NP_003385.2:p.Arg351=
XM_011538721.1:c.685C=	XP_011537023.1:p.Arg229=
XM_011538722.1:c.685C=	XP_011537024.1:p.Arg229=
XM_011538724.1:c.*329C=	XP_011537026.1:n.*329C=
XM_017019919.1:c.685C=	XP_016875408.1:p.Arg229=
XM_024449179.1:c.685C=	XP_024304947.1:p.Arg229=
NM_003394.4:c.1051C= MANE Select	NP_003385.2:p.Arg351=