Canonical Allele Identifier: CA1328961442
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1944522749
gnomAD v4: 2-218882053-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882053G>A , CM000664.2:g.218882053G>A GRCh38
NC_000002.11:g.219746775G>A , CM000664.1:g.219746775G>A GRCh37
NC_000002.10:g.219455019G>A NCBI36
NG_012179.1:g.6521G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-108G>A MANE Select ENSP00000258411.3:n.114-108G>A
ENST00000258411.7:c.114-108G>A ENSP00000258411.3:n.114-108G>A
NM_025216.2:c.114-108G>A NP_079492.2:n.114-108G>A
XM_011511928.1:c.63-108G>A XP_011510230.1:n.63-108G>A
XM_011511929.1:c.18-108G>A XP_011510231.1:n.18-108G>A
XM_011511930.1:c.114-108G>A XP_011510232.1:n.114-108G>A
XM_011511929.2:c.18-108G>A XP_011510231.1:n.18-108G>A
NM_025216.3:c.114-108G>A MANE Select NP_079492.2:n.114-108G>A
Search 100 bp 5'
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