Canonical Allele Identifier: CA1939222085
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1846312966

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117525008A>G , CM000672.2:g.117525008A>G GRCh38
NC_000010.10:g.119284519A>G , CM000672.1:g.119284519A>G GRCh37
NC_000010.9:g.119274509A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002791.2:n.574+19298T>C
NR_144378.1:n.493+17089T>C