Canonical Allele Identifier: CA2408512587

Gene: WNT7B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.45967859A= , CM000684.2:g.45967859A=	GRCh38
NC_000022.10:g.46363739A= , CM000684.1:g.46363739A=	GRCh37
NC_000022.9:g.44742403A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_058238.3:c.71+8825T= MANE Select	NP_478679.1:n.71+8825T=
ENST00000339464.9:c.71+8825T= MANE Select	ENSP00000341032.4:n.71+8825T=
NM_058238.2:c.71+8825T=	NP_478679.1:n.71+8825T=
ENST00000339464.8:c.71+8825T=	ENSP00000341032.4:n.71+8825T=
ENST00000409496.7:c.83+4296T=	ENSP00000386546.3:n.83+4296T=
ENST00000410058.1:c.71+8825T=	ENSP00000387217.1:n.71+8825T=
ENST00000410089.5:c.23+7686T=	ENSP00000386781.1:n.23+7686T=
ENST00000428540.1:c.-131+7831T=	ENSP00000392750.1:n.-131+7831T=
XM_011530366.1:c.83+4296T=	XP_011528668.1:n.83+4296T=