Canonical Allele Identifier: CA3918060

Gene: CNR1

Linked Data

• dbSNP Id: rs749565225
• ExAC: 6:88853570 C / G
• gnomAD v2: 6-88853570-C-G
• gnomAD v3: 6-88143851-C-G
• gnomAD v4: 6-88143851-C-G
• MyVariant Identifiers: chr6:g.88853570C>G (hg19) ; chr6:g.88143851C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88143851C>G , CM000668.2:g.88143851C>G	GRCh38
NC_000006.11:g.88853570C>G , CM000668.1:g.88853570C>G	GRCh37
NC_000006.10:g.88910289C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000362094.6:c.1257G>C	ENSP00000355418.5:n.1257G>C
ENST00000369499.3:c.*5G>C	ENSP00000358511.2:n.*5G>C
ENST00000369501.3:c.*5G>C MANE Select	ENSP00000358513.2:n.*5G>C
ENST00000428600.3:c.*5G>C	ENSP00000412192.2:n.*5G>C
ENST00000468898.2:c.1325G>C	ENSP00000420188.1:n.1325G>C
ENST00000549890.2:c.*5G>C	ENSP00000446819.1:n.*5G>C
ENST00000551417.2:c.*5G>C	ENSP00000446702.2:n.*5G>C
ENST00000369499.2:c.*5G>C	ENSP00000358511.2:n.*5G>C
ENST00000369501.2:c.*5G>C	ENSP00000358513.2:n.*5G>C
ENST00000549890.1:c.*5G>C	ENSP00000446819.1:n.*5G>C
NM_001160226.1:c.*5G>C	NP_001153698.1:n.*5G>C
NM_001160258.1:c.*5G>C	NP_001153730.1:n.*5G>C
NM_001160259.1:c.*5G>C	NP_001153731.1:n.*5G>C
NM_016083.4:c.*5G>C	NP_057167.2:n.*5G>C
NM_033181.3:c.*5G>C	NP_149421.2:n.*5G>C
XM_005248650.3:c.*5G>C	XP_005248707.1:n.*5G>C
XM_006715330.2:c.*5G>C	XP_006715393.1:n.*5G>C
XM_011535424.1:c.*5G>C	XP_011533726.1:n.*5G>C
XM_011535425.1:c.*5G>C	XP_011533727.1:n.*5G>C
XM_011535426.1:c.*5G>C	XP_011533728.1:n.*5G>C
XM_011535427.1:c.*5G>C	XP_011533729.1:n.*5G>C
XM_011535428.1:c.*5G>C	XP_011533730.1:n.*5G>C
NM_001160226.2:c.*5G>C	NP_001153698.1:n.*5G>C
NM_001160258.2:c.*5G>C	NP_001153730.1:n.*5G>C
NM_001160259.2:c.*5G>C	NP_001153731.1:n.*5G>C
NM_001365869.1:c.*5G>C	NP_001352798.1:n.*5G>C
NM_001365870.1:c.*5G>C	NP_001352799.1:n.*5G>C
NM_001365872.1:c.*5G>C	NP_001352801.1:n.*5G>C
NM_001365874.1:c.*5G>C	NP_001352803.1:n.*5G>C
NM_016083.5:c.*5G>C	NP_057167.2:n.*5G>C
NM_033181.4:c.*5G>C	NP_149421.2:n.*5G>C
XM_006715330.3:c.*5G>C	XP_006715393.1:n.*5G>C
XM_011535425.2:c.*5G>C	XP_011533727.1:n.*5G>C
XM_017010240.2:c.*5G>C	XP_016865729.1:n.*5G>C
NM_001160226.3:c.*5G>C	NP_001153698.1:n.*5G>C
NM_001160258.3:c.*5G>C	NP_001153730.1:n.*5G>C
NM_001160259.3:c.*5G>C	NP_001153731.1:n.*5G>C
NM_001365869.2:c.*5G>C	NP_001352798.1:n.*5G>C
NM_001365870.2:c.*5G>C	NP_001352799.1:n.*5G>C
NM_001365872.2:c.*5G>C	NP_001352801.1:n.*5G>C
NM_001365874.2:c.*5G>C	NP_001352803.1:n.*5G>C
NM_001370545.1:c.*5G>C	NP_001357474.1:n.*5G>C
NM_001370546.1:c.*5G>C	NP_001357475.1:n.*5G>C
NM_001370547.1:c.*5G>C	NP_001357476.1:n.*5G>C
NM_016083.6:c.*5G>C MANE Select	NP_057167.2:n.*5G>C
NM_001365874.3:c.*5G>C	NP_001352803.1:n.*5G>C