Canonical Allele Identifier: CA65849782
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs912489477
gnomAD v2: 2-219746436-G-A
gnomAD v3: 2-218881714-G-A
gnomAD v4: 2-218881714-G-A
MyVariant Identifiers: chr2:g.219746436G>A (hg19) chr2:g.218881714G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881714G>A , CM000664.2:g.218881714G>A GRCh38
NC_000002.11:g.219746436G>A , CM000664.1:g.219746436G>A GRCh37
NC_000002.10:g.219454680G>A NCBI36
NG_012179.1:g.6182G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-447G>A MANE Select ENSP00000258411.3:n.114-447G>A
ENST00000258411.7:c.114-447G>A ENSP00000258411.3:n.114-447G>A
NM_025216.2:c.114-447G>A NP_079492.2:n.114-447G>A
XM_011511928.1:c.62+247G>A XP_011510230.1:n.62+247G>A
XM_011511929.1:c.18-447G>A XP_011510231.1:n.18-447G>A
XM_011511930.1:c.114-447G>A XP_011510232.1:n.114-447G>A
XM_011511929.2:c.18-447G>A XP_011510231.1:n.18-447G>A
NM_025216.3:c.114-447G>A MANE Select NP_079492.2:n.114-447G>A
Search 100 bp 5'
Search 100 bp 3'