Canonical Allele Identifier: CA215023062
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1043639155

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524821T>C , CM000672.2:g.117524821T>C GRCh38
NC_000010.10:g.119284332T>C , CM000672.1:g.119284332T>C GRCh37
NC_000010.9:g.119274322T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_002791.2:n.574+19485A>G
NR_144378.1:n.493+17276A>G