Canonical Allele Identifier: CA2113860
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs745962060
ExAC: 2:219746979 G / C
gnomAD v2: 2-219746979-G-C
gnomAD v4: 2-218882257-G-C
MyVariant Identifiers: chr2:g.219746979G>C (hg19) chr2:g.218882257G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882257G>C , CM000664.2:g.218882257G>C GRCh38
NC_000002.11:g.219746979G>C , CM000664.1:g.219746979G>C GRCh37
NC_000002.10:g.219455223G>C NCBI36
NG_012179.1:g.6725G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.210G>C MANE Select ENSP00000258411.3:p.Arg70=
ENST00000258411.7:c.210G>C ENSP00000258411.3:p.Arg70=
ENST00000458582.1:c.97G>C
NM_025216.2:c.210G>C NP_079492.2:p.Arg70=
XM_011511928.1:c.159G>C XP_011510230.1:p.Arg53=
XM_011511929.1:c.114G>C XP_011510231.1:p.Arg38=
XM_011511930.1:c.210G>C XP_011510232.1:p.Arg70=
XM_011511929.2:c.114G>C XP_011510231.1:p.Arg38=
NM_025216.3:c.210G>C MANE Select NP_079492.2:p.Arg70=
Search 100 bp 5'
Search 100 bp 3'