Canonical Allele Identifier: CA2113864
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 3190701
ClinVar RCV Id: RCV004483109
dbSNP Id: rs761027045
ExAC: 2:219746999 G / A
gnomAD v2: 2-219746999-G-A
gnomAD v3: 2-218882277-G-A
gnomAD v4: 2-218882277-G-A
MyVariant Identifiers: chr2:g.219746999G>A (hg19) chr2:g.218882277G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882277G>A , CM000664.2:g.218882277G>A GRCh38
NC_000002.11:g.219746999G>A , CM000664.1:g.219746999G>A GRCh37
NC_000002.10:g.219455243G>A NCBI36
NG_012179.1:g.6745G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.230G>A MANE Select ENSP00000258411.3:p.Arg77His
ENST00000258411.7:c.230G>A ENSP00000258411.3:p.Arg77His
ENST00000458582.1:c.117G>A
NM_025216.2:c.230G>A NP_079492.2:p.Arg77His
XM_011511928.1:c.179G>A XP_011510230.1:p.Arg60His
XM_011511929.1:c.134G>A XP_011510231.1:p.Arg45His
XM_011511930.1:c.230G>A XP_011510232.1:p.Arg77His
XM_011511929.2:c.134G>A XP_011510231.1:p.Arg45His
NM_025216.3:c.230G>A MANE Select NP_079492.2:p.Arg77His
Search 100 bp 5'
Search 100 bp 3'