Canonical Allele Identifier: CA686857

Gene: CNR2

Linked Data

• dbSNP Id: rs769611593
• ExAC: 1:24201921 G / T
• gnomAD v2: 1-24201921-G-T
• gnomAD v4: 1-23875431-G-T
• MyVariant Identifiers: chr1:g.24201921G>T (hg19) ; chr1:g.23875431G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23875431G>T , CM000663.2:g.23875431G>T	GRCh38
NC_000001.10:g.24201921G>T , CM000663.1:g.24201921G>T	GRCh37
NC_000001.9:g.24074508G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374472.5:c.187C>A MANE Select	ENSP00000363596.4:p.Gln63Lys
ENST00000374472.4:c.187C>A	ENSP00000363596.4:p.Gln63Lys
NM_001841.2:c.187C>A	NP_001832.1:p.Gln63Lys
XM_005245736.3:c.187C>A	XP_005245793.1:p.Gln63Lys
XM_011540627.1:c.187C>A	XP_011538929.1:p.Gln63Lys
XM_011540628.1:c.187C>A	XP_011538930.1:p.Gln63Lys
XM_011540629.1:c.187C>A	XP_011538931.1:p.Gln63Lys
XM_011540629.3:c.187C>A	XP_011538931.1:p.Gln63Lys
XM_017000261.2:c.187C>A	XP_016855750.1:p.Gln63Lys
NM_001841.3:c.187C>A MANE Select	NP_001832.1:p.Gln63Lys