Canonical Allele Identifier: CA660461046
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1387495733
MyVariant Identifiers: chr10:g.119284451C>T (hg19) chr10:g.117524940C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524940C>T , CM000672.2:g.117524940C>T GRCh38
NC_000010.10:g.119284451C>T , CM000672.1:g.119284451C>T GRCh37
NC_000010.9:g.119274441C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19366G>A
NR_144378.1:n.493+17157G>A
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