Canonical Allele Identifier: CA65850197

Gene: WNT10A

Linked Data

• dbSNP Id: rs569675304
• gnomAD v3: 2-218882128-A-C
• gnomAD v4: 2-218882128-A-C
• MyVariant Identifiers: chr2:g.219746850A>C (hg19) ; chr2:g.218882128A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882128A>C , CM000664.2:g.218882128A>C	GRCh38
NC_000002.11:g.219746850A>C , CM000664.1:g.219746850A>C	GRCh37
NC_000002.10:g.219455094A>C	NCBI36
NG_012179.1:g.6596A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-33A>C MANE Select	ENSP00000258411.3:n.114-33A>C
ENST00000258411.7:c.114-33A>C	ENSP00000258411.3:n.114-33A>C
NM_025216.2:c.114-33A>C	NP_079492.2:n.114-33A>C
XM_011511928.1:c.63-33A>C	XP_011510230.1:n.63-33A>C
XM_011511929.1:c.18-33A>C	XP_011510231.1:n.18-33A>C
XM_011511930.1:c.114-33A>C	XP_011510232.1:n.114-33A>C
XM_011511929.2:c.18-33A>C	XP_011510231.1:n.18-33A>C
NM_025216.3:c.114-33A>C MANE Select	NP_079492.2:n.114-33A>C