Canonical Allele Identifier: CA12408699
Gene: CNR1 HGNC NCBI

Linked Data

dbSNP Id: rs806377

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88149004T>C , CM000668.2:g.88149004T>C GRCh38
NC_000006.11:g.88858723T>C , CM000668.1:g.88858723T>C GRCh37
NC_000006.10:g.88915442T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369499.2:c.-63-3667A>G ENSP00000358511.2:p.=
ENST00000369501.2:c.-63-3667A>G ENSP00000358513.2:p.=
ENST00000428600.2:c.-63-3667A>G ENSP00000412192.2:p.=
ENST00000551417.1:c.-206-1198A>G ENSP00000446702.1:p.=
NM_001160226.1:c.-206-1198A>G NP_001153698.1:p.=
NM_001160258.1:c.-206-1198A>G NP_001153730.1:p.=
NM_001160259.1:c.-63-3667A>G NP_001153731.1:p.=
NM_016083.4:c.-63-3667A>G NP_057167.2:p.=
XM_005248650.3:c.-254-1198A>G XP_005248707.1:p.=
XM_006715330.2:c.-63-3667A>G XP_006715393.1:p.=
XM_011535424.1:c.-254-1198A>G XP_011533726.1:p.=
XM_011535425.1:c.-254-1198A>G XP_011533727.1:p.=
XM_011535426.1:c.-254-1198A>G XP_011533728.1:p.=
XM_011535427.1:c.-254-1198A>G XP_011533729.1:p.=
XM_011535428.1:c.-63-3667A>G XP_011533730.1:p.=
NM_001160226.2:c.-206-1198A>G NP_001153698.1:p.=
NM_001160258.2:c.-206-1198A>G NP_001153730.1:p.=
NM_001160259.2:c.-63-3667A>G NP_001153731.1:p.=
NM_001365869.1:c.-63-3667A>G NP_001352798.1:p.=
NM_001365870.1:c.-254-1198A>G NP_001352799.1:p.=
NM_001365872.1:c.-254-1198A>G NP_001352801.1:p.=
NM_001365874.1:c.-63-3667A>G NP_001352803.1:p.=
NM_016083.5:c.-63-3667A>G NP_057167.2:p.=
XM_006715330.3:c.-63-3667A>G XP_006715393.1:p.=
XM_011535425.2:c.-254-1198A>G XP_011533727.1:p.=
XM_017010240.2:c.-63-3667A>G XP_016865729.1:p.=
NM_001160226.3:c.-206-1198A>G NP_001153698.1:p.=
NM_001160258.3:c.-206-1198A>G NP_001153730.1:p.=
NM_001160259.3:c.-63-3667A>G NP_001153731.1:p.=
NM_001365869.2:c.-63-3667A>G NP_001352798.1:p.=
NM_001365870.2:c.-254-1198A>G NP_001352799.1:p.=
NM_001365872.2:c.-254-1198A>G NP_001352801.1:p.=
NM_001365874.2:c.-63-3667A>G NP_001352803.1:p.=
NM_001370545.1:c.-63-3667A>G NP_001357474.1:p.=
NM_001370546.1:c.-63-3667A>G NP_001357475.1:p.=
NM_001370547.1:c.-254-1198A>G NP_001357476.1:p.=
NM_016083.6:c.-63-3667A>G MANE Select NP_057167.2:p.=
NM_001365874.3:c.-63-3667A>G NP_001352803.1:p.=