Canonical Allele Identifier: CA2789652348
Gene: EMX2OS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524962G>T , CM000672.2:g.117524962G>T GRCh38
NC_000010.10:g.119284473G>T , CM000672.1:g.119284473G>T GRCh37
NC_000010.9:g.119274463G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19344C>A
NR_144378.1:n.493+17135C>A