Canonical Allele Identifier: CA339019865

Gene: CNR2

Linked Data

• dbSNP Id: rs1488942624
• gnomAD v4: 1-23875336-G-C
• MyVariant Identifiers: chr1:g.24201826G>C (hg19) ; chr1:g.23875336G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000374472.5:c.282C>G MANE Select	ENSP00000363596.4:p.Phe94Leu
ENST00000374472.4:c.282C>G	ENSP00000363596.4:p.Phe94Leu
NM_001841.2:c.282C>G	NP_001832.1:p.Phe94Leu
XM_005245736.3:c.282C>G	XP_005245793.1:p.Phe94Leu
XM_011540627.1:c.282C>G	XP_011538929.1:p.Phe94Leu
XM_011540628.1:c.282C>G	XP_011538930.1:p.Phe94Leu
XM_011540629.1:c.282C>G	XP_011538931.1:p.Phe94Leu
XM_011540629.3:c.282C>G	XP_011538931.1:p.Phe94Leu
XM_017000261.2:c.282C>G	XP_016855750.1:p.Phe94Leu
NM_001841.3:c.282C>G MANE Select	NP_001832.1:p.Phe94Leu