Canonical Allele Identifier: CA764944220
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1231302296
gnomAD v3: 2-218893387-C-A
gnomAD v4: 2-218893387-C-A
MyVariant Identifiers: chr2:g.219758109C>A (hg19) chr2:g.218893387C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893387C>A , CM000664.2:g.218893387C>A GRCh38
NC_000002.11:g.219758109C>A , CM000664.1:g.219758109C>A GRCh37
NC_000002.10:g.219466353C>A NCBI36
NG_012179.1:g.17855C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.*116C>A MANE Select ENSP00000258411.3:n.*116C>A
ENST00000258411.7:c.*116C>A ENSP00000258411.3:n.*116C>A
ENST00000489887.1:n.47+120C>A
NM_025216.2:c.*116C>A NP_079492.2:n.*116C>A
XM_011511928.1:c.*116C>A XP_011510230.1:n.*116C>A
XM_011511929.1:c.*116C>A XP_011510231.1:n.*116C>A
XM_011511930.1:c.*90C>A XP_011510232.1:n.*90C>A
XM_011511929.2:c.*116C>A XP_011510231.1:n.*116C>A
NM_025216.3:c.*116C>A MANE Select NP_079492.2:n.*116C>A
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