Canonical Allele Identifier: CA2408515940
Gene: WNT7B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45973866G= , CM000684.2:g.45973866G= GRCh38
NC_000022.10:g.46369746G= , CM000684.1:g.46369746G= GRCh37
NC_000022.9:g.44748410G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339464.9:c.71+2818C= MANE Select ENSP00000341032.4:n.71+2818C=
ENST00000339464.8:c.71+2818C= ENSP00000341032.4:n.71+2818C=
ENST00000410058.1:c.71+2818C= ENSP00000387217.1:n.71+2818C=
ENST00000410089.5:c.23+1679C= ENSP00000386781.1:n.23+1679C=
ENST00000428540.1:c.-131+1824C= ENSP00000392750.1:n.-131+1824C=
NM_058238.2:c.71+2818C= NP_478679.1:n.71+2818C=
NM_058238.3:c.71+2818C= MANE Select NP_478679.1:n.71+2818C=
Search 100 bp 5'
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