Canonical Allele Identifier: CA15727075
Gene: OLR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1050283

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10159690G>A , CM000674.2:g.10159690G>A GRCh38
NC_000012.11:g.10312289G>A , CM000674.1:g.10312289G>A GRCh37
NC_000012.10:g.10203556G>A NCBI36
NG_016743.1:g.17502C>T

Transcript Alleles

HGVS Amino-acid change
NM_001172632.1:c.*326C>T VV NP_001166103.1:p.=
NM_001172633.1:c.*326C>T VV NP_001166104.1:p.=
NM_002543.3:c.*190C>T VV NP_002534.1:p.=
XM_011520682.1:c.*190C>T XP_011518984.1:p.=
XM_011520683.1:c.*342C>T XP_011518985.1:p.=
NM_002543.4:c.*190C>T VV MANE Preferred NP_002534.1:p.=
ENST00000309539.7:c.*190C>T ENSP00000309124.3:p.=
ENST00000432556.6:c.*326C>T ENSP00000405116.2:p.=
ENST00000536989.1:n.547C>T
ENST00000543993.5:c.*326C>T ENSP00000445085.1:p.=
ENST00000544577.5:c.*190C>T ENSP00000444457.1:p.=
ENST00000545927.5:c.*326C>T ENSP00000439251.1:p.=