Canonical Allele Identifier: CA13720198
Gene: OLR1 HGNC NCBI

Linked Data

dbSNP Id: rs1050286

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10158964T>C , CM000674.2:g.10158964T>C GRCh38
NC_000012.11:g.10311563T>C , CM000674.1:g.10311563T>C GRCh37
NC_000012.10:g.10202830T>C NCBI36
NG_016743.1:g.18228A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000309539.8:c.*916A>G MANE Select ENSP00000309124.3:n.*916A>G
ENST00000309539.7:c.*916A>G ENSP00000309124.3:n.*916A>G
NM_001172632.1:c.*1052A>G NP_001166103.1:n.*1052A>G
NM_001172633.1:c.*1052A>G NP_001166104.1:n.*1052A>G
NM_002543.3:c.*916A>G NP_002534.1:n.*916A>G
XM_011520682.1:c.*916A>G XP_011518984.1:n.*916A>G
XM_011520683.1:c.*1068A>G XP_011518985.1:n.*1068A>G
NM_002543.4:c.*916A>G MANE Select NP_002534.1:n.*916A>G
NM_001172632.2:c.*1052A>G NP_001166103.1:n.*1052A>G
NM_001172633.2:c.*1052A>G NP_001166104.1:n.*1052A>G