Canonical Allele Identifier: CA682736921

Gene: OLR1

Linked Data

• dbSNP Id: rs1367116272
• gnomAD v3: 12-10159518-T-A
• gnomAD v4: 12-10159518-T-A
• MyVariant Identifiers: chr12:g.10312117T>A (hg19) ; chr12:g.10159518T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159518T>A , CM000674.2:g.10159518T>A	GRCh38
NC_000012.11:g.10312117T>A , CM000674.1:g.10312117T>A	GRCh37
NC_000012.10:g.10203384T>A	NCBI36
NG_016743.1:g.17674A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.*362A>T MANE Select	ENSP00000309124.3:n.*362A>T
ENST00000309539.7:c.*362A>T	ENSP00000309124.3:n.*362A>T
ENST00000544577.5:c.*362A>T	ENSP00000444457.1:n.*362A>T
NM_001172632.1:c.*498A>T	NP_001166103.1:n.*498A>T
NM_001172633.1:c.*498A>T	NP_001166104.1:n.*498A>T
NM_002543.3:c.*362A>T	NP_002534.1:n.*362A>T
XM_011520682.1:c.*362A>T	XP_011518984.1:n.*362A>T
XM_011520683.1:c.*514A>T	XP_011518985.1:n.*514A>T
NM_002543.4:c.*362A>T MANE Select	NP_002534.1:n.*362A>T
NM_001172632.2:c.*498A>T	NP_001166103.1:n.*498A>T
NM_001172633.2:c.*498A>T	NP_001166104.1:n.*498A>T