Canonical Allele Identifier: CA675280
Gene: WNT4 HGNC NCBI

Linked Data

dbSNP Id: rs761338261
ExAC: 1:22446852 C / T
gnomAD v2: 1-22446852-C-T
gnomAD v4: 1-22120359-C-T
MyVariant Identifiers: chr1:g.22446852C>T (hg19) chr1:g.22120359C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22120359C>T , CM000663.2:g.22120359C>T GRCh38
NC_000001.10:g.22446852C>T , CM000663.1:g.22446852C>T GRCh37
NC_000001.9:g.22319439C>T NCBI36
NG_008974.1:g.27668G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290167.11:c.747G>A MANE Select ENSP00000290167.5:p.Val249=
ENST00000290167.10:c.747G>A ENSP00000290167.5:p.Val249=
NM_030761.4:c.747G>A NP_110388.2:p.Val249=
XM_011541597.1:c.813G>A XP_011539899.1:p.Val271=
XM_011541598.1:c.582G>A XP_011539900.1:p.Val194=
XM_011541597.2:c.813G>A XP_011539899.1:p.Val271=
XM_011541598.2:c.582G>A XP_011539900.1:p.Val194=
NM_030761.5:c.747G>A MANE Select NP_110388.2:p.Val249=
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