Canonical Allele Identifier: CA1939222026
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1846311992

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524878C>T , CM000672.2:g.117524878C>T GRCh38
NC_000010.10:g.119284389C>T , CM000672.1:g.119284389C>T GRCh37
NC_000010.9:g.119274379C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19428G>A
NR_144378.1:n.493+17219G>A