Canonical Allele Identifier: CA829366424

Gene: CNR1

Linked Data

• dbSNP Id: rs1455756853
• gnomAD v3: 6-88163241-C-T
• gnomAD v4: 6-88163241-C-T
• MyVariant Identifiers: chr6:g.88872960C>T (hg19) ; chr6:g.88163241C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163241C>T , CM000668.2:g.88163241C>T	GRCh38
NC_000006.11:g.88872960C>T , CM000668.1:g.88872960C>T	GRCh37
NC_000006.10:g.88929679C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-64+1016G>A	ENSP00000358511.2:n.-64+1016G>A
ENST00000369501.3:c.-64+2562G>A MANE Select	ENSP00000358513.2:n.-64+2562G>A
ENST00000551417.2:c.-207+1016G>A	ENSP00000446702.2:n.-207+1016G>A
ENST00000369499.2:c.-64+1016G>A	ENSP00000358511.2:n.-64+1016G>A
ENST00000369501.2:c.-64+2562G>A	ENSP00000358513.2:n.-64+2562G>A
ENST00000551417.1:c.-207+1016G>A	ENSP00000446702.1:n.-207+1016G>A
NM_001160226.1:c.-207+2562G>A	NP_001153698.1:n.-207+2562G>A
NM_001160258.1:c.-207+1016G>A	NP_001153730.1:n.-207+1016G>A
NM_001160259.1:c.-64+2506G>A	NP_001153731.1:n.-64+2506G>A
NM_016083.4:c.-64+2562G>A	NP_057167.2:n.-64+2562G>A
XM_006715330.2:c.-64+3335G>A	XP_006715393.1:n.-64+3335G>A
XM_011535424.1:c.-255+2562G>A	XP_011533726.1:n.-255+2562G>A
XM_011535425.1:c.-255+1016G>A	XP_011533727.1:n.-255+1016G>A
XM_011535426.1:c.-413+1016G>A	XP_011533728.1:n.-413+1016G>A
XM_011535427.1:c.-366+1016G>A	XP_011533729.1:n.-366+1016G>A
XM_011535428.1:c.-64+1016G>A	XP_011533730.1:n.-64+1016G>A
NM_001160226.2:c.-207+2562G>A	NP_001153698.1:n.-207+2562G>A
NM_001160258.2:c.-207+1016G>A	NP_001153730.1:n.-207+1016G>A
NM_001160259.2:c.-64+2506G>A	NP_001153731.1:n.-64+2506G>A
NM_001365869.1:c.-64+1016G>A	NP_001352798.1:n.-64+1016G>A
NM_001365870.1:c.-255+2562G>A	NP_001352799.1:n.-255+2562G>A
NM_001365872.1:c.-413+1016G>A	NP_001352801.1:n.-413+1016G>A
NM_016083.5:c.-64+2562G>A	NP_057167.2:n.-64+2562G>A
XM_006715330.3:c.-64+3335G>A	XP_006715393.1:n.-64+3335G>A
XM_011535425.2:c.-255+1016G>A	XP_011533727.1:n.-255+1016G>A
XM_017010240.2:c.-64+3949G>A	XP_016865729.1:n.-64+3949G>A
NM_001160226.3:c.-207+2562G>A	NP_001153698.1:n.-207+2562G>A
NM_001160258.3:c.-207+1016G>A	NP_001153730.1:n.-207+1016G>A
NM_001160259.3:c.-64+2506G>A	NP_001153731.1:n.-64+2506G>A
NM_001365869.2:c.-64+1016G>A	NP_001352798.1:n.-64+1016G>A
NM_001365870.2:c.-255+2562G>A	NP_001352799.1:n.-255+2562G>A
NM_001365872.2:c.-413+1016G>A	NP_001352801.1:n.-413+1016G>A
NM_001370545.1:c.-64+3335G>A	NP_001357474.1:n.-64+3335G>A
NM_001370546.1:c.-64+3949G>A	NP_001357475.1:n.-64+3949G>A
NM_001370547.1:c.-255+1016G>A	NP_001357476.1:n.-255+1016G>A
NM_016083.6:c.-64+2562G>A MANE Select	NP_057167.2:n.-64+2562G>A