Canonical Allele Identifier: CA2113866
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs760336599
ExAC: 2:219747016 G / A
gnomAD v2: 2-219747016-G-A
gnomAD v3: 2-218882294-G-A
gnomAD v4: 2-218882294-G-A
MyVariant Identifiers: chr2:g.219747016G>A (hg19) chr2:g.218882294G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882294G>A , CM000664.2:g.218882294G>A GRCh38
NC_000002.11:g.219747016G>A , CM000664.1:g.219747016G>A GRCh37
NC_000002.10:g.219455260G>A NCBI36
NG_012179.1:g.6762G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.247G>A MANE Select ENSP00000258411.3:p.Ala83Thr
ENST00000258411.7:c.247G>A ENSP00000258411.3:p.Ala83Thr
ENST00000458582.1:c.134G>A
NM_025216.2:c.247G>A NP_079492.2:p.Ala83Thr
XM_011511928.1:c.196G>A XP_011510230.1:p.Ala66Thr
XM_011511929.1:c.151G>A XP_011510231.1:p.Ala51Thr
XM_011511930.1:c.247G>A XP_011510232.1:p.Ala83Thr
XM_011511929.2:c.151G>A XP_011510231.1:p.Ala51Thr
NM_025216.3:c.247G>A MANE Select NP_079492.2:p.Ala83Thr
Search 100 bp 5'
Search 100 bp 3'