Canonical Allele Identifier: CA2113856
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 582506
ClinVar RCV Id: RCV000706597 RCV001825402 RCV004544952
dbSNP Id: rs200487809
ExAC: 2:219746974 C / T
gnomAD v2: 2-219746974-C-T
gnomAD v3: 2-218882252-C-T
gnomAD v4: 2-218882252-C-T
MyVariant Identifiers: chr2:g.219746974C>T (hg19) chr2:g.218882252C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882252C>T , CM000664.2:g.218882252C>T GRCh38
NC_000002.11:g.219746974C>T , CM000664.1:g.219746974C>T GRCh37
NC_000002.10:g.219455218C>T NCBI36
NG_012179.1:g.6720C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.205C>T MANE Select ENSP00000258411.3:p.Arg69Trp
ENST00000258411.7:c.205C>T ENSP00000258411.3:p.Arg69Trp
ENST00000458582.1:c.92C>T
NM_025216.2:c.205C>T NP_079492.2:p.Arg69Trp
XM_011511928.1:c.154C>T XP_011510230.1:p.Arg52Trp
XM_011511929.1:c.109C>T XP_011510231.1:p.Arg37Trp
XM_011511930.1:c.205C>T XP_011510232.1:p.Arg69Trp
XM_011511929.2:c.109C>T XP_011510231.1:p.Arg37Trp
NM_025216.3:c.205C>T MANE Select NP_079492.2:p.Arg69Trp
Search 100 bp 5'
Search 100 bp 3'