Canonical Allele Identifier: CA2589144280
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs2133957547

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524798A>G , CM000672.2:g.117524798A>G GRCh38
NC_000010.10:g.119284309A>G , CM000672.1:g.119284309A>G GRCh37
NC_000010.9:g.119274299A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19508T>C
NR_144378.1:n.493+17299T>C