Canonical Allele Identifier: CA932986893
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1846312026

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524883G>A , CM000672.2:g.117524883G>A GRCh38
NC_000010.10:g.119284394G>A , CM000672.1:g.119284394G>A GRCh37
NC_000010.9:g.119274384G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19423C>T
NR_144378.1:n.493+17214C>T