Canonical Allele Identifier: CA65849749
Gene: WNT10A HGNC NCBI

Linked Data

dbSNP Id: rs1003218016
MyVariant Identifiers: chr2:g.219746411T>C (hg19) chr2:g.218881689T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218881689T>C , CM000664.2:g.218881689T>C GRCh38
NC_000002.11:g.219746411T>C , CM000664.1:g.219746411T>C GRCh37
NC_000002.10:g.219454655T>C NCBI36
NG_012179.1:g.6157T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.114-472T>C MANE Select ENSP00000258411.3:n.114-472T>C
ENST00000258411.7:c.114-472T>C ENSP00000258411.3:n.114-472T>C
NM_025216.2:c.114-472T>C NP_079492.2:n.114-472T>C
XM_011511928.1:c.62+222T>C XP_011510230.1:n.62+222T>C
XM_011511929.1:c.18-472T>C XP_011510231.1:n.18-472T>C
XM_011511930.1:c.114-472T>C XP_011510232.1:n.114-472T>C
XM_011511929.2:c.18-472T>C XP_011510231.1:n.18-472T>C
NM_025216.3:c.114-472T>C MANE Select NP_079492.2:n.114-472T>C
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