Canonical Allele Identifier: CA682736994

Gene: OLR1

Linked Data

• dbSNP Id: rs1320748735
• gnomAD v3: 12-10159719-G-T
• gnomAD v4: 12-10159719-G-T
• MyVariant Identifiers: chr12:g.10312318G>T (hg19) ; chr12:g.10159719G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159719G>T , CM000674.2:g.10159719G>T	GRCh38
NC_000012.11:g.10312318G>T , CM000674.1:g.10312318G>T	GRCh37
NC_000012.10:g.10203585G>T	NCBI36
NG_016743.1:g.17473C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*161C>A MANE Select	ENSP00000309124.3:n.*161C>A
ENST00000309539.7:c.*161C>A	ENSP00000309124.3:n.*161C>A
ENST00000432556.6:c.*297C>A	ENSP00000405116.2:n.*297C>A
ENST00000536989.1:n.518C>A
ENST00000543993.5:c.*297C>A	ENSP00000445085.1:n.*297C>A
ENST00000544577.5:c.*161C>A	ENSP00000444457.1:n.*161C>A
ENST00000545927.5:c.*297C>A	ENSP00000439251.1:n.*297C>A
NM_001172632.1:c.*297C>A	NP_001166103.1:n.*297C>A
NM_001172633.1:c.*297C>A	NP_001166104.1:n.*297C>A
NM_002543.3:c.*161C>A	NP_002534.1:n.*161C>A
XM_011520682.1:c.*161C>A	XP_011518984.1:n.*161C>A
XM_011520683.1:c.*313C>A	XP_011518985.1:n.*313C>A
NM_002543.4:c.*161C>A MANE Select	NP_002534.1:n.*161C>A
NM_001172632.2:c.*297C>A	NP_001166103.1:n.*297C>A
NM_001172633.2:c.*297C>A	NP_001166104.1:n.*297C>A