Canonical Allele Identifier: CA913530355
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1564746088

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524987A>C , CM000672.2:g.117524987A>C GRCh38
NC_000010.10:g.119284498A>C , CM000672.1:g.119284498A>C GRCh37
NC_000010.9:g.119274488A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002791.2:n.574+19319T>G
NR_144378.1:n.493+17110T>G