Canonical Allele Identifier: CA10718875
Gene: WNT4 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.22143914C>T
GRCh37 chr1:g.22470407C>T
gnomAD v2:
1:22470407 C / T
gnomAD v3:
1:22143914 C / T
gnomAD v4:
chr1-22143914-C-T
Joint Max Group AF 0.4915463 (EAS)
Genomes Max Group AF 0.49154607 (EAS)
Exomes Max Group AF 0.13269396 (NFE)
dbSNP:
56318008
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22143914C>T , CM000663.2:g.22143914C>T GRCh38
NC_000001.10:g.22470407C>T , CM000663.1:g.22470407C>T GRCh37
NC_000001.9:g.22342994C>T NCBI36
NG_008974.1:g.4113G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000441048.1:c.-271G>A ENSP00000388925.1:n.-271G>A
XM_011541598.1:c.-271G>A XP_011539900.1:n.-271G>A
XR_947049.1:n.82+1010C>T
XR_947050.1:n.53+2909C>T
XR_947051.1:n.47+923C>T
XR_947053.1:n.82+1010C>T
XR_947054.1:n.82+1010C>T
XR_947055.1:n.82+1010C>T
XM_011541598.2:c.-271G>A XP_011539900.1:n.-271G>A
XR_001737923.1:n.52+923C>T
XR_001737924.1:n.52+923C>T
XR_001737925.1:n.52+923C>T
XR_947051.2:n.52+923C>T
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