Canonical Allele Identifier: CA339020400

Gene: CNR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23875430T>A , CM000663.2:g.23875430T>A	GRCh38
NC_000001.10:g.24201920T>A , CM000663.1:g.24201920T>A	GRCh37
NC_000001.9:g.24074507T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374472.5:c.188A>T MANE Select	ENSP00000363596.4:p.Gln63Leu
ENST00000374472.4:c.188A>T	ENSP00000363596.4:p.Gln63Leu
NM_001841.2:c.188A>T	NP_001832.1:p.Gln63Leu
XM_005245736.3:c.188A>T	XP_005245793.1:p.Gln63Leu
XM_011540627.1:c.188A>T	XP_011538929.1:p.Gln63Leu
XM_011540628.1:c.188A>T	XP_011538930.1:p.Gln63Leu
XM_011540629.1:c.188A>T	XP_011538931.1:p.Gln63Leu
XM_011540629.3:c.188A>T	XP_011538931.1:p.Gln63Leu
XM_017000261.2:c.188A>T	XP_016855750.1:p.Gln63Leu
NM_001841.3:c.188A>T MANE Select	NP_001832.1:p.Gln63Leu