Canonical Allele Identifier: CA232805999

Gene: OLR1

Linked Data

• dbSNP Id: rs935182876
• gnomAD v3: 12-10159720-G-A
• gnomAD v4: 12-10159720-G-A
• MyVariant Identifiers: chr12:g.10312319G>A (hg19) ; chr12:g.10159720G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159720G>A , CM000674.2:g.10159720G>A	GRCh38
NC_000012.11:g.10312319G>A , CM000674.1:g.10312319G>A	GRCh37
NC_000012.10:g.10203586G>A	NCBI36
NG_016743.1:g.17472C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*160C>T MANE Select	ENSP00000309124.3:n.*160C>T
ENST00000309539.7:c.*160C>T	ENSP00000309124.3:n.*160C>T
ENST00000432556.6:c.*296C>T	ENSP00000405116.2:n.*296C>T
ENST00000536989.1:n.517C>T
ENST00000543993.5:c.*296C>T	ENSP00000445085.1:n.*296C>T
ENST00000544577.5:c.*160C>T	ENSP00000444457.1:n.*160C>T
ENST00000545927.5:c.*296C>T	ENSP00000439251.1:n.*296C>T
NM_001172632.1:c.*296C>T	NP_001166103.1:n.*296C>T
NM_001172633.1:c.*296C>T	NP_001166104.1:n.*296C>T
NM_002543.3:c.*160C>T	NP_002534.1:n.*160C>T
XM_011520682.1:c.*160C>T	XP_011518984.1:n.*160C>T
XM_011520683.1:c.*312C>T	XP_011518985.1:n.*312C>T
NM_002543.4:c.*160C>T MANE Select	NP_002534.1:n.*160C>T
NM_001172632.2:c.*296C>T	NP_001166103.1:n.*296C>T
NM_001172633.2:c.*296C>T	NP_001166104.1:n.*296C>T