Canonical Allele Identifier: CA143229429

Gene: CNR1

Linked Data

• dbSNP Id: rs746092221
• MyVariant Identifiers: chr6:g.88873155A>C (hg19) ; chr6:g.88163436A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88163436A>C , CM000668.2:g.88163436A>C	GRCh38
NC_000006.11:g.88873155A>C , CM000668.1:g.88873155A>C	GRCh37
NC_000006.10:g.88929874A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369499.3:c.-64+821T>G	ENSP00000358511.2:n.-64+821T>G
ENST00000369501.3:c.-64+2367T>G MANE Select	ENSP00000358513.2:n.-64+2367T>G
ENST00000551417.2:c.-207+821T>G	ENSP00000446702.2:n.-207+821T>G
ENST00000369499.2:c.-64+821T>G	ENSP00000358511.2:n.-64+821T>G
ENST00000369501.2:c.-64+2367T>G	ENSP00000358513.2:n.-64+2367T>G
ENST00000551417.1:c.-207+821T>G	ENSP00000446702.1:n.-207+821T>G
NM_001160226.1:c.-207+2367T>G	NP_001153698.1:n.-207+2367T>G
NM_001160258.1:c.-207+821T>G	NP_001153730.1:n.-207+821T>G
NM_001160259.1:c.-64+2311T>G	NP_001153731.1:n.-64+2311T>G
NM_016083.4:c.-64+2367T>G	NP_057167.2:n.-64+2367T>G
XM_006715330.2:c.-64+3140T>G	XP_006715393.1:n.-64+3140T>G
XM_011535424.1:c.-255+2367T>G	XP_011533726.1:n.-255+2367T>G
XM_011535425.1:c.-255+821T>G	XP_011533727.1:n.-255+821T>G
XM_011535426.1:c.-413+821T>G	XP_011533728.1:n.-413+821T>G
XM_011535427.1:c.-366+821T>G	XP_011533729.1:n.-366+821T>G
XM_011535428.1:c.-64+821T>G	XP_011533730.1:n.-64+821T>G
NM_001160226.2:c.-207+2367T>G	NP_001153698.1:n.-207+2367T>G
NM_001160258.2:c.-207+821T>G	NP_001153730.1:n.-207+821T>G
NM_001160259.2:c.-64+2311T>G	NP_001153731.1:n.-64+2311T>G
NM_001365869.1:c.-64+821T>G	NP_001352798.1:n.-64+821T>G
NM_001365870.1:c.-255+2367T>G	NP_001352799.1:n.-255+2367T>G
NM_001365872.1:c.-413+821T>G	NP_001352801.1:n.-413+821T>G
NM_016083.5:c.-64+2367T>G	NP_057167.2:n.-64+2367T>G
XM_006715330.3:c.-64+3140T>G	XP_006715393.1:n.-64+3140T>G
XM_011535425.2:c.-255+821T>G	XP_011533727.1:n.-255+821T>G
XM_017010240.2:c.-64+3754T>G	XP_016865729.1:n.-64+3754T>G
NM_001160226.3:c.-207+2367T>G	NP_001153698.1:n.-207+2367T>G
NM_001160258.3:c.-207+821T>G	NP_001153730.1:n.-207+821T>G
NM_001160259.3:c.-64+2311T>G	NP_001153731.1:n.-64+2311T>G
NM_001365869.2:c.-64+821T>G	NP_001352798.1:n.-64+821T>G
NM_001365870.2:c.-255+2367T>G	NP_001352799.1:n.-255+2367T>G
NM_001365872.2:c.-413+821T>G	NP_001352801.1:n.-413+821T>G
NM_001370545.1:c.-64+3140T>G	NP_001357474.1:n.-64+3140T>G
NM_001370546.1:c.-64+3754T>G	NP_001357475.1:n.-64+3754T>G
NM_001370547.1:c.-255+821T>G	NP_001357476.1:n.-255+821T>G
NM_016083.6:c.-64+2367T>G MANE Select	NP_057167.2:n.-64+2367T>G