Canonical Allele Identifier: CA10614197
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 334379
ClinVar RCV Id: RCV000302946 RCV000342611 RCV000396361
dbSNP Id: rs556182426
gnomAD v2: 2-219745318-T-G
gnomAD v3: 2-218880596-T-G
gnomAD v4: 2-218880596-T-G
MyVariant Identifiers: chr2:g.219745318T>G (hg19) chr2:g.218880596T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218880596T>G , CM000664.2:g.218880596T>G GRCh38
NC_000002.11:g.219745318T>G , CM000664.1:g.219745318T>G GRCh37
NC_000002.10:g.219453562T>G NCBI36
NG_012179.1:g.5064T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.7:c.-400T>G ENSP00000258411.3:n.-400T>G
NM_025216.2:c.-400T>G NP_079492.2:n.-400T>G
XM_011511929.1:c.18-1565T>G XP_011510231.1:n.18-1565T>G
XM_011511929.2:c.18-1565T>G XP_011510231.1:n.18-1565T>G
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