Canonical Allele Identifier: CA753637940

Gene: WNT7B

Linked Data

• dbSNP Id: rs1184882364
• MyVariant Identifiers: chr22:g.46369743T>A (hg19) ; chr22:g.45973863T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.45973863T>A , CM000684.2:g.45973863T>A	GRCh38
NC_000022.10:g.46369743T>A , CM000684.1:g.46369743T>A	GRCh37
NC_000022.9:g.44748407T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000339464.9:c.71+2821A>T MANE Select	ENSP00000341032.4:n.71+2821A>T
ENST00000339464.8:c.71+2821A>T	ENSP00000341032.4:n.71+2821A>T
ENST00000410058.1:c.71+2821A>T	ENSP00000387217.1:n.71+2821A>T
ENST00000410089.5:c.23+1682A>T	ENSP00000386781.1:n.23+1682A>T
ENST00000428540.1:c.-131+1827A>T	ENSP00000392750.1:n.-131+1827A>T
NM_058238.2:c.71+2821A>T	NP_478679.1:n.71+2821A>T
NM_058238.3:c.71+2821A>T MANE Select	NP_478679.1:n.71+2821A>T