Canonical Allele Identifier: CA2408515927
Gene: WNT7B HGNC NCBI

Linked Data

dbSNP Id: rs1932500445
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Genomic Alleles

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

Transcript Alleles

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