Canonical Allele Identifier: CA1939222081
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1846312922

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524997C>T , CM000672.2:g.117524997C>T GRCh38
NC_000010.10:g.119284508C>T , CM000672.1:g.119284508C>T GRCh37
NC_000010.9:g.119274498C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19309G>A
NR_144378.1:n.493+17100G>A