Canonical Allele Identifier: CA2113865

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 704869
• ClinVar RCV Id: RCV000875071 ; RCV001138801 ; RCV001138802 ; RCV001138803
• dbSNP Id: rs199802454
• ExAC: 2:219747003 C / T
• gnomAD v2: 2-219747003-C-T
• gnomAD v3: 2-218882281-C-T
• gnomAD v4: 2-218882281-C-T
• MyVariant Identifiers: chr2:g.219747003C>T (hg19) ; chr2:g.218882281C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882281C>T , CM000664.2:g.218882281C>T	GRCh38
NC_000002.11:g.219747003C>T , CM000664.1:g.219747003C>T	GRCh37
NC_000002.10:g.219455247C>T	NCBI36
NG_012179.1:g.6749C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.234C>T MANE Select	ENSP00000258411.3:p.His78=
ENST00000258411.7:c.234C>T	ENSP00000258411.3:p.His78=
ENST00000458582.1:c.121C>T
NM_025216.2:c.234C>T	NP_079492.2:p.His78=
XM_011511928.1:c.183C>T	XP_011510230.1:p.His61=
XM_011511929.1:c.138C>T	XP_011510231.1:p.His46=
XM_011511930.1:c.234C>T	XP_011510232.1:p.His78=
XM_011511929.2:c.138C>T	XP_011510231.1:p.His46=
NM_025216.3:c.234C>T MANE Select	NP_079492.2:p.His78=