Canonical Allele Identifier: CA1939221994
Gene: EMX2OS HGNC NCBI

Linked Data

dbSNP Id: rs1564746046

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117524762C>T , CM000672.2:g.117524762C>T GRCh38
NC_000010.10:g.119284273C>T , CM000672.1:g.119284273C>T GRCh37
NC_000010.9:g.119274263C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002791.2:n.574+19544G>A
NR_144378.1:n.493+17335G>A