Canonical Allele Identifier: CA2408515935

Gene: WNT7B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.45973845A= , CM000684.2:g.45973845A=	GRCh38
NC_000022.10:g.46369725A= , CM000684.1:g.46369725A=	GRCh37
NC_000022.9:g.44748389A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000339464.9:c.71+2839T= MANE Select	ENSP00000341032.4:n.71+2839T=
ENST00000339464.8:c.71+2839T=	ENSP00000341032.4:n.71+2839T=
ENST00000410058.1:c.71+2839T=	ENSP00000387217.1:n.71+2839T=
ENST00000410089.5:c.23+1700T=	ENSP00000386781.1:n.23+1700T=
ENST00000428540.1:c.-131+1845T=	ENSP00000392750.1:n.-131+1845T=
NM_058238.2:c.71+2839T=	NP_478679.1:n.71+2839T=
NM_058238.3:c.71+2839T= MANE Select	NP_478679.1:n.71+2839T=