Canonical Allele Identifier: CA416691398

Gene: CNR2

Linked Data

• MyVariant Identifiers: chr1:g.24201826G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23875336G>A , CM000663.2:g.23875336G>A	GRCh38
NC_000001.10:g.24201826G>A , CM000663.1:g.24201826G>A	GRCh37
NC_000001.9:g.24074413G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374472.5:c.282C>T MANE Select	ENSP00000363596.4:p.Phe94=
ENST00000374472.4:c.282C>T	ENSP00000363596.4:p.Phe94=
NM_001841.2:c.282C>T	NP_001832.1:p.Phe94=
XM_005245736.3:c.282C>T	XP_005245793.1:p.Phe94=
XM_011540627.1:c.282C>T	XP_011538929.1:p.Phe94=
XM_011540628.1:c.282C>T	XP_011538930.1:p.Phe94=
XM_011540629.1:c.282C>T	XP_011538931.1:p.Phe94=
XM_011540629.3:c.282C>T	XP_011538931.1:p.Phe94=
XM_017000261.2:c.282C>T	XP_016855750.1:p.Phe94=
NM_001841.3:c.282C>T MANE Select	NP_001832.1:p.Phe94=