Canonical Allele Identifier: CA1026256005
Gene: WNT7B HGNC NCBI

Linked Data

dbSNP Id: rs1932500225
gnomAD v3: 22-45973814-G-C
gnomAD v4: 22-45973814-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45973814G>C , CM000684.2:g.45973814G>C GRCh38
NC_000022.10:g.46369694G>C , CM000684.1:g.46369694G>C GRCh37
NC_000022.9:g.44748358G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339464.9:c.71+2870C>G MANE Select ENSP00000341032.4:n.71+2870C>G
ENST00000339464.8:c.71+2870C>G ENSP00000341032.4:n.71+2870C>G
ENST00000410058.1:c.71+2870C>G ENSP00000387217.1:n.71+2870C>G
ENST00000410089.5:c.23+1731C>G ENSP00000386781.1:n.23+1731C>G
ENST00000428540.1:c.-131+1876C>G ENSP00000392750.1:n.-131+1876C>G
NM_058238.2:c.71+2870C>G NP_478679.1:n.71+2870C>G
NM_058238.3:c.71+2870C>G MANE Select NP_478679.1:n.71+2870C>G
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