Canonical Allele Identifier: CA2113863
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs748131786
ExAC: 2:219746998 C / T
gnomAD v2: 2-219746998-C-T
gnomAD v3: 2-218882276-C-T
gnomAD v4: 2-218882276-C-T
COSMIC: COSM573500
MyVariant Identifiers: chr2:g.219746998C>T (hg19) chr2:g.218882276C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882276C>T , CM000664.2:g.218882276C>T GRCh38
NC_000002.11:g.219746998C>T , CM000664.1:g.219746998C>T GRCh37
NC_000002.10:g.219455242C>T NCBI36
NG_012179.1:g.6744C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.229C>T MANE Select ENSP00000258411.3:p.Arg77Cys
ENST00000258411.7:c.229C>T ENSP00000258411.3:p.Arg77Cys
ENST00000458582.1:c.116C>T
NM_025216.2:c.229C>T NP_079492.2:p.Arg77Cys
XM_011511928.1:c.178C>T XP_011510230.1:p.Arg60Cys
XM_011511929.1:c.133C>T XP_011510231.1:p.Arg45Cys
XM_011511930.1:c.229C>T XP_011510232.1:p.Arg77Cys
XM_011511929.2:c.133C>T XP_011510231.1:p.Arg45Cys
NM_025216.3:c.229C>T MANE Select NP_079492.2:p.Arg77Cys
Search 100 bp 5'
Search 100 bp 3'