Canonical Allele Identifier: CA2408515926
Gene: WNT7B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45973828T= , CM000684.2:g.45973828T= GRCh38
NC_000022.10:g.46369708T= , CM000684.1:g.46369708T= GRCh37
NC_000022.9:g.44748372T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339464.9:c.71+2856A= MANE Select ENSP00000341032.4:n.71+2856A=
ENST00000339464.8:c.71+2856A= ENSP00000341032.4:n.71+2856A=
ENST00000410058.1:c.71+2856A= ENSP00000387217.1:n.71+2856A=
ENST00000410089.5:c.23+1717A= ENSP00000386781.1:n.23+1717A=
ENST00000428540.1:c.-131+1862A= ENSP00000392750.1:n.-131+1862A=
NM_058238.2:c.71+2856A= NP_478679.1:n.71+2856A=
NM_058238.3:c.71+2856A= MANE Select NP_478679.1:n.71+2856A=
Search 100 bp 5'
Search 100 bp 3'