Canonical Allele Identifier: CA1939222000
Gene: EMX2OS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524776A= , CM000672.2:g.117524776A= GRCh38
NC_000010.10:g.119284287A= , CM000672.1:g.119284287A= GRCh37
NC_000010.9:g.119274277A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19530T=
NR_144378.1:n.493+17321T=