Canonical Allele Identifier: CA603264382

Gene: OLR1

Linked Data

• dbSNP Id: rs1293352545
• gnomAD v2: 12-10312220-A-T
• gnomAD v3: 12-10159621-A-T
• gnomAD v4: 12-10159621-A-T
• MyVariant Identifiers: chr12:g.10312220A>T (hg19) ; chr12:g.10159621A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159621A>T , CM000674.2:g.10159621A>T	GRCh38
NC_000012.11:g.10312220A>T , CM000674.1:g.10312220A>T	GRCh37
NC_000012.10:g.10203487A>T	NCBI36
NG_016743.1:g.17571T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*259T>A MANE Select	ENSP00000309124.3:n.*259T>A
ENST00000309539.7:c.*259T>A	ENSP00000309124.3:n.*259T>A
ENST00000543993.5:c.*395T>A	ENSP00000445085.1:n.*395T>A
ENST00000544577.5:c.*259T>A	ENSP00000444457.1:n.*259T>A
ENST00000545927.5:c.*395T>A	ENSP00000439251.1:n.*395T>A
NM_001172632.1:c.*395T>A	NP_001166103.1:n.*395T>A
NM_001172633.1:c.*395T>A	NP_001166104.1:n.*395T>A
NM_002543.3:c.*259T>A	NP_002534.1:n.*259T>A
XM_011520682.1:c.*259T>A	XP_011518984.1:n.*259T>A
XM_011520683.1:c.*411T>A	XP_011518985.1:n.*411T>A
NM_002543.4:c.*259T>A MANE Select	NP_002534.1:n.*259T>A
NM_001172632.2:c.*395T>A	NP_001166103.1:n.*395T>A
NM_001172633.2:c.*395T>A	NP_001166104.1:n.*395T>A