Canonical Allele Identifier: CA660460984
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1338622328
MyVariant Identifiers: chr10:g.119284307G>A (hg19) chr10:g.117524796G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524796G>A , CM000672.2:g.117524796G>A GRCh38
NC_000010.10:g.119284307G>A , CM000672.1:g.119284307G>A GRCh37
NC_000010.9:g.119274297G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19510C>T
NR_144378.1:n.493+17301C>T
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