Canonical Allele Identifier: CA16617469
Gene: WNT10A HGNC NCBI

Linked Data

ClinVar Variation Id: 423769
ClinVar RCV Id: RCV000483296
dbSNP Id: rs1064796619
gnomAD v3: 2-218882289-T-C
gnomAD v4: 2-218882289-T-C
MyVariant Identifiers: chr2:g.219747011T>C (hg19) chr2:g.218882289T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882289T>C , CM000664.2:g.218882289T>C GRCh38
NC_000002.11:g.219747011T>C , CM000664.1:g.219747011T>C GRCh37
NC_000002.10:g.219455255T>C NCBI36
NG_012179.1:g.6757T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.242T>C MANE Select ENSP00000258411.3:p.Val81Ala
ENST00000258411.7:c.242T>C ENSP00000258411.3:p.Val81Ala
ENST00000458582.1:c.129T>C
NM_025216.2:c.242T>C NP_079492.2:p.Val81Ala
XM_011511928.1:c.191T>C XP_011510230.1:p.Val64Ala
XM_011511929.1:c.146T>C XP_011510231.1:p.Val49Ala
XM_011511930.1:c.242T>C XP_011510232.1:p.Val81Ala
XM_011511929.2:c.146T>C XP_011510231.1:p.Val49Ala
NM_025216.3:c.242T>C MANE Select NP_079492.2:p.Val81Ala
Search 100 bp 5'
Search 100 bp 3'