Canonical Allele Identifier: CA1939221964
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs938757675

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524705G>C , CM000672.2:g.117524705G>C GRCh38
NC_000010.10:g.119284216G>C , CM000672.1:g.119284216G>C GRCh37
NC_000010.9:g.119274206G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002791.2:n.574+19601C>G
NR_144378.1:n.493+17392C>G