Canonical Allele Identifier: CA2617607477
Gene: OLR1 HGNC NCBI

Linked Data

gnomAD v4: 12-10159531-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10159531G>T , CM000674.2:g.10159531G>T GRCh38
NC_000012.11:g.10312130G>T , CM000674.1:g.10312130G>T GRCh37
NC_000012.10:g.10203397G>T NCBI36
NG_016743.1:g.17661C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309539.8:c.*349C>A MANE Select ENSP00000309124.3:n.*349C>A
ENST00000309539.7:c.*349C>A ENSP00000309124.3:n.*349C>A
ENST00000544577.5:c.*349C>A ENSP00000444457.1:n.*349C>A
NM_001172632.1:c.*485C>A NP_001166103.1:n.*485C>A
NM_001172633.1:c.*485C>A NP_001166104.1:n.*485C>A
NM_002543.3:c.*349C>A NP_002534.1:n.*349C>A
XM_011520682.1:c.*349C>A XP_011518984.1:n.*349C>A
XM_011520683.1:c.*501C>A XP_011518985.1:n.*501C>A
NM_002543.4:c.*349C>A MANE Select NP_002534.1:n.*349C>A
NM_001172632.2:c.*485C>A NP_001166103.1:n.*485C>A
NM_001172633.2:c.*485C>A NP_001166104.1:n.*485C>A
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