Canonical Allele Identifier: CA143229397

Gene: CNR1

Linked Data

• dbSNP Id: rs777136119
• gnomAD v2: 6-88872795-C-A
• gnomAD v3: 6-88163076-C-A
• gnomAD v4: 6-88163076-C-A
• MyVariant Identifiers: chr6:g.88872795C>A (hg19) ; chr6:g.88163076C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163076C>A , CM000668.2:g.88163076C>A	GRCh38
NC_000006.11:g.88872795C>A , CM000668.1:g.88872795C>A	GRCh37
NC_000006.10:g.88929514C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369499.3:c.-64+1181G>T	ENSP00000358511.2:n.-64+1181G>T
ENST00000369501.3:c.-64+2727G>T MANE Select	ENSP00000358513.2:n.-64+2727G>T
ENST00000551417.2:c.-207+1181G>T	ENSP00000446702.2:n.-207+1181G>T
ENST00000369499.2:c.-64+1181G>T	ENSP00000358511.2:n.-64+1181G>T
ENST00000369501.2:c.-64+2727G>T	ENSP00000358513.2:n.-64+2727G>T
ENST00000551417.1:c.-207+1181G>T	ENSP00000446702.1:n.-207+1181G>T
NM_001160226.1:c.-207+2727G>T	NP_001153698.1:n.-207+2727G>T
NM_001160258.1:c.-207+1181G>T	NP_001153730.1:n.-207+1181G>T
NM_001160259.1:c.-64+2671G>T	NP_001153731.1:n.-64+2671G>T
NM_016083.4:c.-64+2727G>T	NP_057167.2:n.-64+2727G>T
XM_006715330.2:c.-64+3500G>T	XP_006715393.1:n.-64+3500G>T
XM_011535424.1:c.-255+2727G>T	XP_011533726.1:n.-255+2727G>T
XM_011535425.1:c.-255+1181G>T	XP_011533727.1:n.-255+1181G>T
XM_011535426.1:c.-413+1181G>T	XP_011533728.1:n.-413+1181G>T
XM_011535427.1:c.-366+1181G>T	XP_011533729.1:n.-366+1181G>T
XM_011535428.1:c.-64+1181G>T	XP_011533730.1:n.-64+1181G>T
NM_001160226.2:c.-207+2727G>T	NP_001153698.1:n.-207+2727G>T
NM_001160258.2:c.-207+1181G>T	NP_001153730.1:n.-207+1181G>T
NM_001160259.2:c.-64+2671G>T	NP_001153731.1:n.-64+2671G>T
NM_001365869.1:c.-64+1181G>T	NP_001352798.1:n.-64+1181G>T
NM_001365870.1:c.-255+2727G>T	NP_001352799.1:n.-255+2727G>T
NM_001365872.1:c.-413+1181G>T	NP_001352801.1:n.-413+1181G>T
NM_001365874.1:c.-183G>T	NP_001352803.1:n.-183G>T
NM_016083.5:c.-64+2727G>T	NP_057167.2:n.-64+2727G>T
XM_006715330.3:c.-64+3500G>T	XP_006715393.1:n.-64+3500G>T
XM_011535425.2:c.-255+1181G>T	XP_011533727.1:n.-255+1181G>T
XM_017010240.2:c.-64+4114G>T	XP_016865729.1:n.-64+4114G>T
NM_001160226.3:c.-207+2727G>T	NP_001153698.1:n.-207+2727G>T
NM_001160258.3:c.-207+1181G>T	NP_001153730.1:n.-207+1181G>T
NM_001160259.3:c.-64+2671G>T	NP_001153731.1:n.-64+2671G>T
NM_001365869.2:c.-64+1181G>T	NP_001352798.1:n.-64+1181G>T
NM_001365870.2:c.-255+2727G>T	NP_001352799.1:n.-255+2727G>T
NM_001365872.2:c.-413+1181G>T	NP_001352801.1:n.-413+1181G>T
NM_001370545.1:c.-64+3500G>T	NP_001357474.1:n.-64+3500G>T
NM_001370546.1:c.-64+4114G>T	NP_001357475.1:n.-64+4114G>T
NM_001370547.1:c.-255+1181G>T	NP_001357476.1:n.-255+1181G>T
NM_016083.6:c.-64+2727G>T MANE Select	NP_057167.2:n.-64+2727G>T