Canonical Allele Identifier: CA660461017
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1316826566
MyVariant Identifiers: chr10:g.119284407C>A (hg19) chr10:g.117524896C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524896C>A , CM000672.2:g.117524896C>A GRCh38
NC_000010.10:g.119284407C>A , CM000672.1:g.119284407C>A GRCh37
NC_000010.9:g.119274397C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19410G>T
NR_144378.1:n.493+17201G>T
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