Canonical Allele Identifier: CA1939222054
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1846312475

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524935del , CM000672.2:g.117524935del GRCh38
NC_000010.10:g.119284446del , CM000672.1:g.119284446del GRCh37
NC_000010.9:g.119274436del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19371del
NR_144378.1:n.493+17162del