Canonical Allele Identifier: CA2113851
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1139770
ClinVar RCV Id: RCV001476605
dbSNP Id: rs758914779
ExAC: 2:219746937 T / C
gnomAD v2: 2-219746937-T-C
gnomAD v3: 2-218882215-T-C
gnomAD v4: 2-218882215-T-C
MyVariant Identifiers: chr2:g.219746937T>C (hg19) chr2:g.218882215T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882215T>C , CM000664.2:g.218882215T>C GRCh38
NC_000002.11:g.219746937T>C , CM000664.1:g.219746937T>C GRCh37
NC_000002.10:g.219455181T>C NCBI36
NG_012179.1:g.6683T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.168T>C MANE Select ENSP00000258411.3:p.Asn56=
ENST00000258411.7:c.168T>C ENSP00000258411.3:p.Asn56=
ENST00000458582.1:c.55T>C
NM_025216.2:c.168T>C NP_079492.2:p.Asn56=
XM_011511928.1:c.117T>C XP_011510230.1:p.Asn39=
XM_011511929.1:c.72T>C XP_011510231.1:p.Asn24=
XM_011511930.1:c.168T>C XP_011510232.1:p.Asn56=
XM_011511929.2:c.72T>C XP_011510231.1:p.Asn24=
NM_025216.3:c.168T>C MANE Select NP_079492.2:p.Asn56=
Search 100 bp 5'
Search 100 bp 3'