Canonical Allele Identifier: CA2034911703

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48965999G= , CM000674.2:g.48965999G=	GRCh38
NC_000012.11:g.49359782G= , CM000674.1:g.49359782G=	GRCh37
NC_000012.10:g.47646049G=	NCBI36
NG_023347.1:g.10860C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.*96C= MANE Select	ENSP00000301061.4:n.*96C=
ENST00000301061.8:c.*96C=	ENSP00000301061.4:n.*96C=
ENST00000403957.5:c.*548C=	ENSP00000385980.1:n.*548C=
ENST00000407467.5:c.*548C=	ENSP00000384691.1:n.*548C=
NM_003394.3:c.*96C=	NP_003385.2:n.*96C=
XM_011538721.1:c.*96C=	XP_011537023.1:n.*96C=
XM_011538722.1:c.*96C=	XP_011537024.1:n.*96C=
XM_017019919.1:c.*96C=	XP_016875408.1:n.*96C=
XM_024449179.1:c.*96C=	XP_024304947.1:n.*96C=
NM_003394.4:c.*96C= MANE Select	NP_003385.2:n.*96C=