Canonical Allele Identifier: CA2113990
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 427045
ClinVar RCV Id: RCV000489933 RCV001037834 RCV003323568 RCV003972817
dbSNP Id: rs775380022
ExAC: 2:219754990 G / A
gnomAD v2: 2-219754990-G-A
gnomAD v4: 2-218890268-G-A
MyVariant Identifiers: chr2:g.219754990G>A (hg19) chr2:g.218890268G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218890268G>A , CM000664.2:g.218890268G>A GRCh38
NC_000002.11:g.219754990G>A , CM000664.1:g.219754990G>A GRCh37
NC_000002.10:g.219463234G>A NCBI36
NG_012179.1:g.14736G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258411.8:c.661G>A MANE Select ENSP00000258411.3:p.Gly221Arg
ENST00000258411.7:c.661G>A ENSP00000258411.3:p.Gly221Arg
ENST00000458582.1:c.264-2506G>A
NM_025216.2:c.661G>A NP_079492.2:p.Gly221Arg
XM_011511928.1:c.610G>A XP_011510230.1:p.Gly204Arg
XM_011511929.1:c.565G>A XP_011510231.1:p.Gly189Arg
XM_011511930.1:c.377-2506G>A XP_011510232.1:n.377-2506G>A
XM_011511929.2:c.565G>A XP_011510231.1:p.Gly189Arg
NM_025216.3:c.661G>A MANE Select NP_079492.2:p.Gly221Arg
Search 100 bp 5'
Search 100 bp 3'