Canonical Allele Identifier: CA65850311
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1153106
ClinVar RCV Id: RCV001494653
dbSNP Id: rs904675306
MyVariant Identifiers: chr2:g.219746970G>C (hg19) chr2:g.218882248G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882248G>C , CM000664.2:g.218882248G>C GRCh38
NC_000002.11:g.219746970G>C , CM000664.1:g.219746970G>C GRCh37
NC_000002.10:g.219455214G>C NCBI36
NG_012179.1:g.6716G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.201G>C MANE Select ENSP00000258411.3:p.Leu67=
ENST00000258411.7:c.201G>C ENSP00000258411.3:p.Leu67=
ENST00000458582.1:c.88G>C
NM_025216.2:c.201G>C NP_079492.2:p.Leu67=
XM_011511928.1:c.150G>C XP_011510230.1:p.Leu50=
XM_011511929.1:c.105G>C XP_011510231.1:p.Leu35=
XM_011511930.1:c.201G>C XP_011510232.1:p.Leu67=
XM_011511929.2:c.105G>C XP_011510231.1:p.Leu35=
NM_025216.3:c.201G>C MANE Select NP_079492.2:p.Leu67=
Search 100 bp 5'
Search 100 bp 3'