Canonical Allele Identifier: CA65850304
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs947767429
MyVariant Identifiers: chr2:g.219746967C>A (hg19) chr2:g.218882245C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882245C>A , CM000664.2:g.218882245C>A GRCh38
NC_000002.11:g.219746967C>A , CM000664.1:g.219746967C>A GRCh37
NC_000002.10:g.219455211C>A NCBI36
NG_012179.1:g.6713C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.198C>A MANE Select ENSP00000258411.3:p.Gly66=
ENST00000258411.7:c.198C>A ENSP00000258411.3:p.Gly66=
ENST00000458582.1:c.85C>A
NM_025216.2:c.198C>A NP_079492.2:p.Gly66=
XM_011511928.1:c.147C>A XP_011510230.1:p.Gly49=
XM_011511929.1:c.102C>A XP_011510231.1:p.Gly34=
XM_011511930.1:c.198C>A XP_011510232.1:p.Gly66=
XM_011511929.2:c.102C>A XP_011510231.1:p.Gly34=
NM_025216.3:c.198C>A MANE Select NP_079492.2:p.Gly66=
Search 100 bp 5'
Search 100 bp 3'