Canonical Allele Identifier: CA596259550

Gene: EMX2OS

Linked Data

• dbSNP Id: rs149117720
• gnomAD v2: 10-119284438-C-G
• gnomAD v3: 10-117524927-C-G
• gnomAD v4: 10-117524927-C-G
• MyVariant Identifiers: chr10:g.119284438C>G (hg19) ; chr10:g.117524927C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117524927C>G , CM000672.2:g.117524927C>G	GRCh38
NC_000010.10:g.119284438C>G , CM000672.1:g.119284438C>G	GRCh37
NC_000010.9:g.119274428C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_002791.2:n.574+19379G>C
NR_144378.1:n.493+17170G>C