Canonical Allele Identifier: CA339019891

Gene: CNR2

Linked Data

• MyVariant Identifiers: chr1:g.24201828A>C (hg19) ; chr1:g.23875338A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23875338A>C , CM000663.2:g.23875338A>C	GRCh38
NC_000001.10:g.24201828A>C , CM000663.1:g.24201828A>C	GRCh37
NC_000001.9:g.24074415A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374472.5:c.280T>G MANE Select	ENSP00000363596.4:p.Phe94Val
ENST00000374472.4:c.280T>G	ENSP00000363596.4:p.Phe94Val
NM_001841.2:c.280T>G	NP_001832.1:p.Phe94Val
XM_005245736.3:c.280T>G	XP_005245793.1:p.Phe94Val
XM_011540627.1:c.280T>G	XP_011538929.1:p.Phe94Val
XM_011540628.1:c.280T>G	XP_011538930.1:p.Phe94Val
XM_011540629.1:c.280T>G	XP_011538931.1:p.Phe94Val
XM_011540629.3:c.280T>G	XP_011538931.1:p.Phe94Val
XM_017000261.2:c.280T>G	XP_016855750.1:p.Phe94Val
NM_001841.3:c.280T>G MANE Select	NP_001832.1:p.Phe94Val