Canonical Allele Identifier: CA431416447

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944526191
• gnomAD v3: 2-218882236-A-G
• gnomAD v4: 2-218882236-A-G
• MyVariant Identifiers: chr2:g.219746958A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882236A>G , CM000664.2:g.218882236A>G	GRCh38
NC_000002.11:g.219746958A>G , CM000664.1:g.219746958A>G	GRCh37
NC_000002.10:g.219455202A>G	NCBI36
NG_012179.1:g.6704A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.189A>G MANE Select	ENSP00000258411.3:p.Thr63=
ENST00000258411.7:c.189A>G	ENSP00000258411.3:p.Thr63=
ENST00000458582.1:c.76A>G
NM_025216.2:c.189A>G	NP_079492.2:p.Thr63=
XM_011511928.1:c.138A>G	XP_011510230.1:p.Thr46=
XM_011511929.1:c.93A>G	XP_011510231.1:p.Thr31=
XM_011511930.1:c.189A>G	XP_011510232.1:p.Thr63=
XM_011511929.2:c.93A>G	XP_011510231.1:p.Thr31=
NM_025216.3:c.189A>G MANE Select	NP_079492.2:p.Thr63=