Canonical Allele Identifier: CA232805879

Gene: OLR1

Linked Data

• dbSNP Id: rs190216641
• gnomAD v3: 12-10159544-T-C
• gnomAD v4: 12-10159544-T-C
• MyVariant Identifiers: chr12:g.10312143T>C (hg19) ; chr12:g.10159544T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10159544T>C , CM000674.2:g.10159544T>C	GRCh38
NC_000012.11:g.10312143T>C , CM000674.1:g.10312143T>C	GRCh37
NC_000012.10:g.10203410T>C	NCBI36
NG_016743.1:g.17648A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000309539.8:c.*336A>G MANE Select	ENSP00000309124.3:n.*336A>G
ENST00000309539.7:c.*336A>G	ENSP00000309124.3:n.*336A>G
ENST00000544577.5:c.*336A>G	ENSP00000444457.1:n.*336A>G
NM_001172632.1:c.*472A>G	NP_001166103.1:n.*472A>G
NM_001172633.1:c.*472A>G	NP_001166104.1:n.*472A>G
NM_002543.3:c.*336A>G	NP_002534.1:n.*336A>G
XM_011520682.1:c.*336A>G	XP_011518984.1:n.*336A>G
XM_011520683.1:c.*488A>G	XP_011518985.1:n.*488A>G
NM_002543.4:c.*336A>G MANE Select	NP_002534.1:n.*336A>G
NM_001172632.2:c.*472A>G	NP_001166103.1:n.*472A>G
NM_001172633.2:c.*472A>G	NP_001166104.1:n.*472A>G