Canonical Allele Identifier: CA2114122
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs767517592
ExAC: 2:219757906 C / G
gnomAD v2: 2-219757906-C-G
gnomAD v4: 2-218893184-C-G
MyVariant Identifiers: chr2:g.219757906C>G (hg19) chr2:g.218893184C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893184C>G , CM000664.2:g.218893184C>G GRCh38
NC_000002.11:g.219757906C>G , CM000664.1:g.219757906C>G GRCh37
NC_000002.10:g.219466150C>G NCBI36
NG_012179.1:g.17652C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1167C>G MANE Select ENSP00000258411.3:p.Ser389Arg
ENST00000258411.7:c.1167C>G ENSP00000258411.3:p.Ser389Arg
NM_025216.2:c.1167C>G NP_079492.2:p.Ser389Arg
XM_011511928.1:c.1116C>G XP_011510230.1:p.Ser372Arg
XM_011511929.1:c.1071C>G XP_011510231.1:p.Ser357Arg
XM_011511930.1:c.787C>G XP_011510232.1:p.Arg263Gly
XM_011511929.2:c.1071C>G XP_011510231.1:p.Ser357Arg
NM_025216.3:c.1167C>G MANE Select NP_079492.2:p.Ser389Arg
Search 100 bp 5'
Search 100 bp 3'