Canonical Allele Identifier: CA19289506

Gene: CNR2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23875429_23875430delinsCC , CM000663.2:g.23875429_23875430delinsCC	GRCh38
NC_000001.10:g.24201919_24201920delinsCC , CM000663.1:g.24201919_24201920delinsCC	GRCh37
NC_000001.9:g.24074506_24074507delinsCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374472.5:c.188_189delinsGG MANE Select	ENSP00000363596.4:p.Gln63Arg
ENST00000374472.4:c.188_189delinsGG	ENSP00000363596.4:p.Gln63Arg
NM_001841.2:c.188_189delinsGG	NP_001832.1:p.Gln63Arg
XM_005245736.3:c.188_189delinsGG	XP_005245793.1:p.Gln63Arg
XM_011540627.1:c.188_189delinsGG	XP_011538929.1:p.Gln63Arg
XM_011540628.1:c.188_189delinsGG	XP_011538930.1:p.Gln63Arg
XM_011540629.1:c.188_189delinsGG	XP_011538931.1:p.Gln63Arg
XM_011540629.3:c.188_189delinsGG	XP_011538931.1:p.Gln63Arg
XM_017000261.2:c.188_189delinsGG	XP_016855750.1:p.Gln63Arg
NM_001841.3:c.188_189delinsGG MANE Select	NP_001832.1:p.Gln63Arg