Canonical Allele Identifier: CA215023074

Gene: EMX2OS

Linked Data

• dbSNP Id: rs530522688
• gnomAD v2: 10-119284424-A-T
• gnomAD v3: 10-117524913-A-T
• gnomAD v4: 10-117524913-A-T
• MyVariant Identifiers: chr10:g.119284424A>T (hg19) ; chr10:g.117524913A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117524913A>T , CM000672.2:g.117524913A>T	GRCh38
NC_000010.10:g.119284424A>T , CM000672.1:g.119284424A>T	GRCh37
NC_000010.9:g.119274414A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_002791.2:n.574+19393T>A
NR_144378.1:n.493+17184T>A