Canonical Allele Identifier: CA65849935
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1024966271
MyVariant Identifiers: chr2:g.219746559C>A (hg19) chr2:g.218881837C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881837C>A , CM000664.2:g.218881837C>A GRCh38
NC_000002.11:g.219746559C>A , CM000664.1:g.219746559C>A GRCh37
NC_000002.10:g.219454803C>A NCBI36
NG_012179.1:g.6305C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-324C>A MANE Select ENSP00000258411.3:n.114-324C>A
ENST00000258411.7:c.114-324C>A ENSP00000258411.3:n.114-324C>A
NM_025216.2:c.114-324C>A NP_079492.2:n.114-324C>A
XM_011511928.1:c.63-324C>A XP_011510230.1:n.63-324C>A
XM_011511929.1:c.18-324C>A XP_011510231.1:n.18-324C>A
XM_011511930.1:c.114-324C>A XP_011510232.1:n.114-324C>A
XM_011511929.2:c.18-324C>A XP_011510231.1:n.18-324C>A
NM_025216.3:c.114-324C>A MANE Select NP_079492.2:n.114-324C>A
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