Canonical Allele Identifier: CA596259548
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1221013518

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524887T>A , CM000672.2:g.117524887T>A GRCh38
NC_000010.10:g.119284398T>A , CM000672.1:g.119284398T>A GRCh37
NC_000010.9:g.119274388T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002791.2:n.574+19419A>T
NR_144378.1:n.493+17210A>T