Canonical Allele Identifier: CA3918074
Gene: CNR1 HGNC NCBI

Linked Data

dbSNP Id: rs1049353

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88143916C>T , CM000668.2:g.88143916C>T GRCh38
NC_000006.11:g.88853635C>T , CM000668.1:g.88853635C>T GRCh37
NC_000006.10:g.88910354C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000362094.6:n.1192G>A ENSP00000355418.5:n.1192G>A
ENST00000369499.3:c.1359G>A ENSP00000358511.2:p.Thr453=
ENST00000369501.3:c.1359G>A MANE Select ENSP00000358513.2:p.Thr453=
ENST00000428600.3:c.1359G>A ENSP00000412192.2:p.Thr453=
ENST00000468898.2:n.1260G>A ENSP00000420188.1:p.Thr420=
ENST00000549890.2:c.1359G>A ENSP00000446819.1:p.Thr453=
ENST00000551417.2:c.1359G>A ENSP00000446702.2:p.Thr453=
ENST00000362094.5:n.1192G>A ENSP00000355418.5:n.1192G>A
ENST00000369499.2:c.1359G>A ENSP00000358511.2:p.Thr453=
ENST00000369501.2:c.1359G>A ENSP00000358513.2:p.Thr453=
ENST00000428600.2:c.1359G>A ENSP00000412192.2:p.Thr453=
ENST00000468898.1:n.1260G>A ENSP00000420188.1:p.Thr420=
ENST00000549890.1:c.1359G>A ENSP00000446819.1:p.Thr453=
NM_001160226.1:c.1359G>A NP_001153698.1:p.Thr453=
NM_001160258.1:c.1359G>A NP_001153730.1:p.Thr453=
NM_001160259.1:c.1359G>A NP_001153731.1:p.Thr453=
NM_016083.4:c.1359G>A NP_057167.2:p.Thr453=
NM_033181.3:c.1260G>A NP_149421.2:p.Thr420=
XM_005248650.3:c.1359G>A XP_005248707.1:p.Thr453=
XM_006715330.2:c.1359G>A XP_006715393.1:p.Thr453=
XM_011535424.1:c.1359G>A XP_011533726.1:p.Thr453=
XM_011535425.1:c.1359G>A XP_011533727.1:p.Thr453=
XM_011535426.1:c.1359G>A XP_011533728.1:p.Thr453=
XM_011535427.1:c.1359G>A XP_011533729.1:p.Thr453=
XM_011535428.1:c.1359G>A XP_011533730.1:p.Thr453=
NM_001160226.2:c.1359G>A NP_001153698.1:p.Thr453=
NM_001160258.2:c.1359G>A NP_001153730.1:p.Thr453=
NM_001160259.2:c.1359G>A NP_001153731.1:p.Thr453=
NM_001365869.1:c.1359G>A NP_001352798.1:p.Thr453=
NM_001365870.1:c.1359G>A NP_001352799.1:p.Thr453=
NM_001365872.1:c.1359G>A NP_001352801.1:p.Thr453=
NM_001365874.1:c.1359G>A NP_001352803.1:p.Thr453=
NM_016083.5:c.1359G>A NP_057167.2:p.Thr453=
NM_033181.4:c.1260G>A NP_149421.2:p.Thr420=
XM_006715330.3:c.1359G>A XP_006715393.1:p.Thr453=
XM_011535425.2:c.1359G>A XP_011533727.1:p.Thr453=
XM_017010240.2:c.1359G>A XP_016865729.1:p.Thr453=
NM_001160226.3:c.1359G>A NP_001153698.1:p.Thr453=
NM_001160258.3:c.1359G>A NP_001153730.1:p.Thr453=
NM_001160259.3:c.1359G>A NP_001153731.1:p.Thr453=
NM_001365869.2:c.1359G>A NP_001352798.1:p.Thr453=
NM_001365870.2:c.1359G>A NP_001352799.1:p.Thr453=
NM_001365872.2:c.1359G>A NP_001352801.1:p.Thr453=
NM_001365874.2:c.1359G>A NP_001352803.1:p.Thr453=
NM_001370545.1:c.1359G>A NP_001357474.1:p.Thr453=
NM_001370546.1:c.1359G>A NP_001357475.1:p.Thr453=
NM_001370547.1:c.1359G>A NP_001357476.1:p.Thr453=
NM_016083.6:c.1359G>A MANE Select NP_057167.2:p.Thr453=
NM_001365874.3:c.1359G>A NP_001352803.1:p.Thr453=