Canonical Allele Identifier: CA65850328

Gene: WNT10A

Linked Data

• dbSNP Id: rs147129328
• gnomAD v3: 2-218882250-G-A
• gnomAD v4: 2-218882250-G-A
• MyVariant Identifiers: chr2:g.219746972G>A (hg19) ; chr2:g.218882250G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882250G>A , CM000664.2:g.218882250G>A	GRCh38
NC_000002.11:g.219746972G>A , CM000664.1:g.219746972G>A	GRCh37
NC_000002.10:g.219455216G>A	NCBI36
NG_012179.1:g.6718G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.203G>A MANE Select	ENSP00000258411.3:p.Ser68Asn
ENST00000258411.7:c.203G>A	ENSP00000258411.3:p.Ser68Asn
ENST00000458582.1:c.90G>A
NM_025216.2:c.203G>A	NP_079492.2:p.Ser68Asn
XM_011511928.1:c.152G>A	XP_011510230.1:p.Ser51Asn
XM_011511929.1:c.107G>A	XP_011510231.1:p.Ser36Asn
XM_011511930.1:c.203G>A	XP_011510232.1:p.Ser68Asn
XM_011511929.2:c.107G>A	XP_011510231.1:p.Ser36Asn
NM_025216.3:c.203G>A MANE Select	NP_079492.2:p.Ser68Asn