Canonical Allele Identifier: CA2113837
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1153585
ClinVar RCV Id: RCV001495286 RCV001826330
dbSNP Id: rs149865858
ExAC: 2:219746894 A / G
gnomAD v2: 2-219746894-A-G
gnomAD v3: 2-218882172-A-G
gnomAD v4: 2-218882172-A-G
MyVariant Identifiers: chr2:g.219746894A>G (hg19) chr2:g.218882172A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882172A>G , CM000664.2:g.218882172A>G GRCh38
NC_000002.11:g.219746894A>G , CM000664.1:g.219746894A>G GRCh37
NC_000002.10:g.219455138A>G NCBI36
NG_012179.1:g.6640A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.125A>G MANE Select ENSP00000258411.3:p.Asn42Ser
ENST00000258411.7:c.125A>G ENSP00000258411.3:p.Asn42Ser
ENST00000458582.1:c.12A>G
NM_025216.2:c.125A>G NP_079492.2:p.Asn42Ser
XM_011511928.1:c.74A>G XP_011510230.1:p.Asn25Ser
XM_011511929.1:c.29A>G XP_011510231.1:p.Asn10Ser
XM_011511930.1:c.125A>G XP_011510232.1:p.Asn42Ser
XM_011511929.2:c.29A>G XP_011510231.1:p.Asn10Ser
NM_025216.3:c.125A>G MANE Select NP_079492.2:p.Asn42Ser
Search 100 bp 5'
Search 100 bp 3'