Canonical Allele Identifier: CA2034911664

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965929A= , CM000674.2:g.48965929A=	GRCh38
NC_000012.11:g.49359712A= , CM000674.1:g.49359712A=	GRCh37
NC_000012.10:g.47645979A=	NCBI36
NG_023347.1:g.10930T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*166T= MANE Select	ENSP00000301061.4:n.*166T=
ENST00000301061.8:c.*166T=	ENSP00000301061.4:n.*166T=
ENST00000403957.5:c.*618T=	ENSP00000385980.1:n.*618T=
ENST00000407467.5:c.*618T=	ENSP00000384691.1:n.*618T=
NM_003394.3:c.*166T=	NP_003385.2:n.*166T=
XM_011538721.1:c.*166T=	XP_011537023.1:n.*166T=
XM_011538722.1:c.*166T=	XP_011537024.1:n.*166T=
XM_017019919.1:c.*166T=	XP_016875408.1:n.*166T=
XM_024449179.1:c.*166T=	XP_024304947.1:n.*166T=
NM_003394.4:c.*166T= MANE Select	NP_003385.2:n.*166T=