Canonical Allele Identifier: CA682736946

Gene: OLR1

Linked Data

• dbSNP Id: rs1319054866
• gnomAD v3: 12-10159612-C-G
• gnomAD v4: 12-10159612-C-G
• MyVariant Identifiers: chr12:g.10312211C>G (hg19) ; chr12:g.10159612C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159612C>G , CM000674.2:g.10159612C>G	GRCh38
NC_000012.11:g.10312211C>G , CM000674.1:g.10312211C>G	GRCh37
NC_000012.10:g.10203478C>G	NCBI36
NG_016743.1:g.17580G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309539.8:c.*268G>C MANE Select	ENSP00000309124.3:n.*268G>C
ENST00000309539.7:c.*268G>C	ENSP00000309124.3:n.*268G>C
ENST00000543993.5:c.*404G>C	ENSP00000445085.1:n.*404G>C
ENST00000544577.5:c.*268G>C	ENSP00000444457.1:n.*268G>C
NM_001172632.1:c.*404G>C	NP_001166103.1:n.*404G>C
NM_001172633.1:c.*404G>C	NP_001166104.1:n.*404G>C
NM_002543.3:c.*268G>C	NP_002534.1:n.*268G>C
XM_011520682.1:c.*268G>C	XP_011518984.1:n.*268G>C
XM_011520683.1:c.*420G>C	XP_011518985.1:n.*420G>C
NM_002543.4:c.*268G>C MANE Select	NP_002534.1:n.*268G>C
NM_001172632.2:c.*404G>C	NP_001166103.1:n.*404G>C
NM_001172633.2:c.*404G>C	NP_001166104.1:n.*404G>C