Canonical Allele Identifier: CA12435842
Gene: CNR1 HGNC NCBI

Linked Data

dbSNP Id: rs806380

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88154934A>G , CM000668.2:g.88154934A>G GRCh38
NC_000006.11:g.88864653A>G , CM000668.1:g.88864653A>G GRCh37
NC_000006.10:g.88921372A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369499.2:c.-64+9323T>C ENSP00000358511.2:p.=
ENST00000369501.2:c.-63-9597T>C ENSP00000358513.2:p.=
ENST00000428600.2:c.-64+8023T>C ENSP00000412192.2:p.=
ENST00000551417.1:c.-206-7128T>C ENSP00000446702.1:p.=
NM_001160226.1:c.-206-7128T>C NP_001153698.1:p.=
NM_001160258.1:c.-206-7128T>C NP_001153730.1:p.=
NM_001160259.1:c.-63-9597T>C NP_001153731.1:p.=
NM_016083.4:c.-63-9597T>C NP_057167.2:p.=
XM_006715330.2:c.-63-9597T>C XP_006715393.1:p.=
XM_011535424.1:c.-254-7128T>C XP_011533726.1:p.=
XM_011535425.1:c.-254-7128T>C XP_011533727.1:p.=
XM_011535426.1:c.-412-4294T>C XP_011533728.1:p.=
XM_011535427.1:c.-365-4341T>C XP_011533729.1:p.=
XM_011535428.1:c.-64+9323T>C XP_011533730.1:p.=
NM_001160226.2:c.-206-7128T>C NP_001153698.1:p.=
NM_001160258.2:c.-206-7128T>C NP_001153730.1:p.=
NM_001160259.2:c.-63-9597T>C NP_001153731.1:p.=
NM_001365869.1:c.-64+9323T>C NP_001352798.1:p.=
NM_001365870.1:c.-254-7128T>C NP_001352799.1:p.=
NM_001365872.1:c.-412-4294T>C NP_001352801.1:p.=
NM_001365874.1:c.-64+8023T>C NP_001352803.1:p.=
NM_016083.5:c.-63-9597T>C NP_057167.2:p.=
XM_006715330.3:c.-63-9597T>C XP_006715393.1:p.=
XM_011535425.2:c.-254-7128T>C XP_011533727.1:p.=
XM_017010240.2:c.-63-9597T>C XP_016865729.1:p.=
NM_001160226.3:c.-206-7128T>C NP_001153698.1:p.=
NM_001160258.3:c.-206-7128T>C NP_001153730.1:p.=
NM_001160259.3:c.-63-9597T>C NP_001153731.1:p.=
NM_001365869.2:c.-64+9323T>C NP_001352798.1:p.=
NM_001365870.2:c.-254-7128T>C NP_001352799.1:p.=
NM_001365872.2:c.-412-4294T>C NP_001352801.1:p.=
NM_001365874.2:c.-64+8023T>C NP_001352803.1:p.=
NM_001370545.1:c.-63-9597T>C NP_001357474.1:p.=
NM_001370546.1:c.-63-9597T>C NP_001357475.1:p.=
NM_001370547.1:c.-254-7128T>C NP_001357476.1:p.=
NM_016083.6:c.-63-9597T>C MANE Select NP_057167.2:p.=
NM_001365874.3:c.-64+8023T>C NP_001352803.1:p.=