Canonical Allele Identifier: CA660460994
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1407373816

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524808G>A , CM000672.2:g.117524808G>A GRCh38
NC_000010.10:g.119284319G>A , CM000672.1:g.119284319G>A GRCh37
NC_000010.9:g.119274309G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19498C>T
NR_144378.1:n.493+17289C>T