Canonical Allele Identifier: CA65849744

Gene: WNT10A

Linked Data

• dbSNP Id: rs886206319
• gnomAD v3: 2-218881688-A-G
• gnomAD v4: 2-218881688-A-G
• MyVariant Identifiers: chr2:g.219746410A>G (hg19) ; chr2:g.218881688A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881688A>G , CM000664.2:g.218881688A>G	GRCh38
NC_000002.11:g.219746410A>G , CM000664.1:g.219746410A>G	GRCh37
NC_000002.10:g.219454654A>G	NCBI36
NG_012179.1:g.6156A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.114-473A>G MANE Select	ENSP00000258411.3:n.114-473A>G
ENST00000258411.7:c.114-473A>G	ENSP00000258411.3:n.114-473A>G
NM_025216.2:c.114-473A>G	NP_079492.2:n.114-473A>G
XM_011511928.1:c.62+221A>G	XP_011510230.1:n.62+221A>G
XM_011511929.1:c.18-473A>G	XP_011510231.1:n.18-473A>G
XM_011511930.1:c.114-473A>G	XP_011510232.1:n.114-473A>G
XM_011511929.2:c.18-473A>G	XP_011510231.1:n.18-473A>G
NM_025216.3:c.114-473A>G MANE Select	NP_079492.2:n.114-473A>G