Canonical Allele Identifier: CA416691425

Gene: CNR2

Linked Data

• MyVariant Identifiers: chr1:g.24201832C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23875342C>G , CM000663.2:g.23875342C>G	GRCh38
NC_000001.10:g.24201832C>G , CM000663.1:g.24201832C>G	GRCh37
NC_000001.9:g.24074419C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374472.5:c.276G>C MANE Select	ENSP00000363596.4:p.Val92=
ENST00000374472.4:c.276G>C	ENSP00000363596.4:p.Val92=
NM_001841.2:c.276G>C	NP_001832.1:p.Val92=
XM_005245736.3:c.276G>C	XP_005245793.1:p.Val92=
XM_011540627.1:c.276G>C	XP_011538929.1:p.Val92=
XM_011540628.1:c.276G>C	XP_011538930.1:p.Val92=
XM_011540629.1:c.276G>C	XP_011538931.1:p.Val92=
XM_011540629.3:c.276G>C	XP_011538931.1:p.Val92=
XM_017000261.2:c.276G>C	XP_016855750.1:p.Val92=
NM_001841.3:c.276G>C MANE Select	NP_001832.1:p.Val92=