Canonical Allele Identifier: CA1939222028
Gene: EMX2OS HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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