Canonical Allele Identifier: CA215023050

Gene: EMX2OS

Linked Data

• dbSNP Id: rs540502455
• gnomAD v3: 10-117524707-G-T
• gnomAD v4: 10-117524707-G-T
• MyVariant Identifiers: chr10:g.119284218G>T (hg19) ; chr10:g.117524707G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117524707G>T , CM000672.2:g.117524707G>T	GRCh38
NC_000010.10:g.119284218G>T , CM000672.1:g.119284218G>T	GRCh37
NC_000010.9:g.119274208G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_002791.2:n.574+19599C>A
NR_144378.1:n.493+17390C>A