Canonical Allele Identifier: CA65919439
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2096855
ClinVar RCV Id: RCV003006212
dbSNP Id: rs866650556
gnomAD v4: 2-218893240-G-A
MyVariant Identifiers: chr2:g.219757962G>A (hg19) chr2:g.218893240G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893240G>A , CM000664.2:g.218893240G>A GRCh38
NC_000002.11:g.219757962G>A , CM000664.1:g.219757962G>A GRCh37
NC_000002.10:g.219466206G>A NCBI36
NG_012179.1:g.17708G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1223G>A MANE Select ENSP00000258411.3:p.Arg408His
ENST00000258411.7:c.1223G>A ENSP00000258411.3:p.Arg408His
ENST00000489887.1:n.20G>A
NM_025216.2:c.1223G>A NP_079492.2:p.Arg408His
XM_011511928.1:c.1172G>A XP_011510230.1:p.Arg391His
XM_011511929.1:c.1127G>A XP_011510231.1:p.Arg376His
XM_011511930.1:c.843G>A XP_011510232.1:p.Pro281=
XM_011511929.2:c.1127G>A XP_011510231.1:p.Arg376His
NM_025216.3:c.1223G>A MANE Select NP_079492.2:p.Arg408His
Search 100 bp 5'
Search 100 bp 3'