Canonical Allele Identifier: CA1091538959
Gene: CNR1 HGNC NCBI

Linked Data

dbSNP Id: rs1778191422
gnomAD v3: 6-88163124-A-G
gnomAD v4: 6-88163124-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88163124A>G , CM000668.2:g.88163124A>G GRCh38
NC_000006.11:g.88872843A>G , CM000668.1:g.88872843A>G GRCh37
NC_000006.10:g.88929562A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369499.3:c.-64+1133T>C ENSP00000358511.2:n.-64+1133T>C
ENST00000369501.3:c.-64+2679T>C MANE Select ENSP00000358513.2:n.-64+2679T>C
ENST00000551417.2:c.-207+1133T>C ENSP00000446702.2:n.-207+1133T>C
ENST00000369499.2:c.-64+1133T>C ENSP00000358511.2:n.-64+1133T>C
ENST00000369501.2:c.-64+2679T>C ENSP00000358513.2:n.-64+2679T>C
ENST00000551417.1:c.-207+1133T>C ENSP00000446702.1:n.-207+1133T>C
NM_001160226.1:c.-207+2679T>C NP_001153698.1:n.-207+2679T>C
NM_001160258.1:c.-207+1133T>C NP_001153730.1:n.-207+1133T>C
NM_001160259.1:c.-64+2623T>C NP_001153731.1:n.-64+2623T>C
NM_016083.4:c.-64+2679T>C NP_057167.2:n.-64+2679T>C
XM_006715330.2:c.-64+3452T>C XP_006715393.1:n.-64+3452T>C
XM_011535424.1:c.-255+2679T>C XP_011533726.1:n.-255+2679T>C
XM_011535425.1:c.-255+1133T>C XP_011533727.1:n.-255+1133T>C
XM_011535426.1:c.-413+1133T>C XP_011533728.1:n.-413+1133T>C
XM_011535427.1:c.-366+1133T>C XP_011533729.1:n.-366+1133T>C
XM_011535428.1:c.-64+1133T>C XP_011533730.1:n.-64+1133T>C
NM_001160226.2:c.-207+2679T>C NP_001153698.1:n.-207+2679T>C
NM_001160258.2:c.-207+1133T>C NP_001153730.1:n.-207+1133T>C
NM_001160259.2:c.-64+2623T>C NP_001153731.1:n.-64+2623T>C
NM_001365869.1:c.-64+1133T>C NP_001352798.1:n.-64+1133T>C
NM_001365870.1:c.-255+2679T>C NP_001352799.1:n.-255+2679T>C
NM_001365872.1:c.-413+1133T>C NP_001352801.1:n.-413+1133T>C
NM_016083.5:c.-64+2679T>C NP_057167.2:n.-64+2679T>C
XM_006715330.3:c.-64+3452T>C XP_006715393.1:n.-64+3452T>C
XM_011535425.2:c.-255+1133T>C XP_011533727.1:n.-255+1133T>C
XM_017010240.2:c.-64+4066T>C XP_016865729.1:n.-64+4066T>C
NM_001160226.3:c.-207+2679T>C NP_001153698.1:n.-207+2679T>C
NM_001160258.3:c.-207+1133T>C NP_001153730.1:n.-207+1133T>C
NM_001160259.3:c.-64+2623T>C NP_001153731.1:n.-64+2623T>C
NM_001365869.2:c.-64+1133T>C NP_001352798.1:n.-64+1133T>C
NM_001365870.2:c.-255+2679T>C NP_001352799.1:n.-255+2679T>C
NM_001365872.2:c.-413+1133T>C NP_001352801.1:n.-413+1133T>C
NM_001370545.1:c.-64+3452T>C NP_001357474.1:n.-64+3452T>C
NM_001370546.1:c.-64+4066T>C NP_001357475.1:n.-64+4066T>C
NM_001370547.1:c.-255+1133T>C NP_001357476.1:n.-255+1133T>C
NM_016083.6:c.-64+2679T>C MANE Select NP_057167.2:n.-64+2679T>C