Canonical Allele Identifier: CA65850125
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs376260386
MyVariant Identifiers: chr2:g.219746803T>G (hg19) chr2:g.218882081T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882081T>G , CM000664.2:g.218882081T>G GRCh38
NC_000002.11:g.219746803T>G , CM000664.1:g.219746803T>G GRCh37
NC_000002.10:g.219455047T>G NCBI36
NG_012179.1:g.6549T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-80T>G MANE Select ENSP00000258411.3:n.114-80T>G
ENST00000258411.7:c.114-80T>G ENSP00000258411.3:n.114-80T>G
NM_025216.2:c.114-80T>G NP_079492.2:n.114-80T>G
XM_011511928.1:c.63-80T>G XP_011510230.1:n.63-80T>G
XM_011511929.1:c.18-80T>G XP_011510231.1:n.18-80T>G
XM_011511930.1:c.114-80T>G XP_011510232.1:n.114-80T>G
XM_011511929.2:c.18-80T>G XP_011510231.1:n.18-80T>G
NM_025216.3:c.114-80T>G MANE Select NP_079492.2:n.114-80T>G
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