Canonical Allele Identifier: CA65850278
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 894811
ClinVar RCV Id: RCV001136561 RCV001136562 RCV001136563
dbSNP Id: rs992196031
MyVariant Identifiers: chr2:g.219746935A>G (hg19) chr2:g.218882213A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882213A>G , CM000664.2:g.218882213A>G GRCh38
NC_000002.11:g.219746935A>G , CM000664.1:g.219746935A>G GRCh37
NC_000002.10:g.219455179A>G NCBI36
NG_012179.1:g.6681A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.166A>G MANE Select ENSP00000258411.3:p.Asn56Asp
ENST00000258411.7:c.166A>G ENSP00000258411.3:p.Asn56Asp
ENST00000458582.1:c.53A>G
NM_025216.2:c.166A>G NP_079492.2:p.Asn56Asp
XM_011511928.1:c.115A>G XP_011510230.1:p.Asn39Asp
XM_011511929.1:c.70A>G XP_011510231.1:p.Asn24Asp
XM_011511930.1:c.166A>G XP_011510232.1:p.Asn56Asp
XM_011511929.2:c.70A>G XP_011510231.1:p.Asn24Asp
NM_025216.3:c.166A>G MANE Select NP_079492.2:p.Asn56Asp
Search 100 bp 5'
Search 100 bp 3'