Canonical Allele Identifier: CA2113836
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs758769542
ExAC: 2:219746889 A / C
gnomAD v2: 2-219746889-A-C
gnomAD v4: 2-218882167-A-C
MyVariant Identifiers: chr2:g.219746889A>C (hg19) chr2:g.218882167A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882167A>C , CM000664.2:g.218882167A>C GRCh38
NC_000002.11:g.219746889A>C , CM000664.1:g.219746889A>C GRCh37
NC_000002.10:g.219455133A>C NCBI36
NG_012179.1:g.6635A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.120A>C MANE Select ENSP00000258411.3:p.Ala40=
ENST00000258411.7:c.120A>C ENSP00000258411.3:p.Ala40=
ENST00000458582.1:c.7A>C
NM_025216.2:c.120A>C NP_079492.2:p.Ala40=
XM_011511928.1:c.69A>C XP_011510230.1:p.Ala23=
XM_011511929.1:c.24A>C XP_011510231.1:p.Ala8=
XM_011511930.1:c.120A>C XP_011510232.1:p.Ala40=
XM_011511929.2:c.24A>C XP_011510231.1:p.Ala8=
NM_025216.3:c.120A>C MANE Select NP_079492.2:p.Ala40=
Search 100 bp 5'
Search 100 bp 3'