Canonical Allele Identifier: CA1939222058
Gene: EMX2OS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524947A= , CM000672.2:g.117524947A= GRCh38
NC_000010.10:g.119284458A= , CM000672.1:g.119284458A= GRCh37
NC_000010.9:g.119274448A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19359T=
NR_144378.1:n.493+17150T=