Canonical Allele Identifier: CA2114125
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs766086207
ExAC: 2:219757923 G / A
gnomAD v2: 2-219757923-G-A
gnomAD v4: 2-218893201-G-A
MyVariant Identifiers: chr2:g.219757923G>A (hg19) chr2:g.218893201G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893201G>A , CM000664.2:g.218893201G>A GRCh38
NC_000002.11:g.219757923G>A , CM000664.1:g.219757923G>A GRCh37
NC_000002.10:g.219466167G>A NCBI36
NG_012179.1:g.17669G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1184G>A MANE Select ENSP00000258411.3:p.Arg395His
ENST00000258411.7:c.1184G>A ENSP00000258411.3:p.Arg395His
NM_025216.2:c.1184G>A NP_079492.2:p.Arg395His
XM_011511928.1:c.1133G>A XP_011510230.1:p.Arg378His
XM_011511929.1:c.1088G>A XP_011510231.1:p.Arg363His
XM_011511930.1:c.804G>A XP_011510232.1:p.Pro268=
XM_011511929.2:c.1088G>A XP_011510231.1:p.Arg363His
NM_025216.3:c.1184G>A MANE Select NP_079492.2:p.Arg395His
Search 100 bp 5'
Search 100 bp 3'