Canonical Allele Identifier: CA1158991555

Gene: CNR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23875436G= , CM000663.2:g.23875436G=	GRCh38
NC_000001.10:g.24201926G= , CM000663.1:g.24201926G=	GRCh37
NC_000001.9:g.24074513G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374472.5:c.182C= MANE Select	ENSP00000363596.4:p.Ser61=
ENST00000374472.4:c.182C=	ENSP00000363596.4:p.Ser61=
NM_001841.2:c.182C=	NP_001832.1:p.Ser61=
XM_005245736.3:c.182C=	XP_005245793.1:p.Ser61=
XM_011540627.1:c.182C=	XP_011538929.1:p.Ser61=
XM_011540628.1:c.182C=	XP_011538930.1:p.Ser61=
XM_011540629.1:c.182C=	XP_011538931.1:p.Ser61=
XM_011540629.3:c.182C=	XP_011538931.1:p.Ser61=
XM_017000261.2:c.182C=	XP_016855750.1:p.Ser61=
NM_001841.3:c.182C= MANE Select	NP_001832.1:p.Ser61=