Canonical Allele Identifier: CA16127390
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1259665
ClinVar RCV Id: RCV001666582
dbSNP Id: rs10180544
gnomAD v2: 2-219746827-T-C
gnomAD v3: 2-218882105-T-C
gnomAD v4: 2-218882105-T-C
MyVariant Identifiers: chr2:g.219746827T>C (hg19) chr2:g.218882105T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882105T>C , CM000664.2:g.218882105T>C GRCh38
NC_000002.11:g.219746827T>C , CM000664.1:g.219746827T>C GRCh37
NC_000002.10:g.219455071T>C NCBI36
NG_012179.1:g.6573T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-56T>C MANE Select ENSP00000258411.3:n.114-56T>C
ENST00000258411.7:c.114-56T>C ENSP00000258411.3:n.114-56T>C
NM_025216.2:c.114-56T>C NP_079492.2:n.114-56T>C
XM_011511928.1:c.63-56T>C XP_011510230.1:n.63-56T>C
XM_011511929.1:c.18-56T>C XP_011510231.1:n.18-56T>C
XM_011511930.1:c.114-56T>C XP_011510232.1:n.114-56T>C
XM_011511929.2:c.18-56T>C XP_011510231.1:n.18-56T>C
NM_025216.3:c.114-56T>C MANE Select NP_079492.2:n.114-56T>C
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