Canonical Allele Identifier: CA232805913

Gene: OLR1

Linked Data

• dbSNP Id: rs181195036
• gnomAD v2: 12-10312203-A-G
• gnomAD v3: 12-10159604-A-G
• gnomAD v4: 12-10159604-A-G
• MyVariant Identifiers: chr12:g.10312203A>G (hg19) ; chr12:g.10159604A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159604A>G , CM000674.2:g.10159604A>G	GRCh38
NC_000012.11:g.10312203A>G , CM000674.1:g.10312203A>G	GRCh37
NC_000012.10:g.10203470A>G	NCBI36
NG_016743.1:g.17588T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*276T>C MANE Select	ENSP00000309124.3:n.*276T>C
ENST00000309539.7:c.*276T>C	ENSP00000309124.3:n.*276T>C
ENST00000543993.5:c.*412T>C	ENSP00000445085.1:n.*412T>C
ENST00000544577.5:c.*276T>C	ENSP00000444457.1:n.*276T>C
NM_001172632.1:c.*412T>C	NP_001166103.1:n.*412T>C
NM_001172633.1:c.*412T>C	NP_001166104.1:n.*412T>C
NM_002543.3:c.*276T>C	NP_002534.1:n.*276T>C
XM_011520682.1:c.*276T>C	XP_011518984.1:n.*276T>C
XM_011520683.1:c.*428T>C	XP_011518985.1:n.*428T>C
NM_002543.4:c.*276T>C MANE Select	NP_002534.1:n.*276T>C
NM_001172632.2:c.*412T>C	NP_001166103.1:n.*412T>C
NM_001172633.2:c.*412T>C	NP_001166104.1:n.*412T>C