Canonical Allele Identifier: CA339020403
Gene: CNR2 HGNC NCBI

Linked Data

dbSNP Id: rs2501432

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23875430T>G , CM000663.2:g.23875430T>G GRCh38
NC_000001.10:g.24201920T>G , CM000663.1:g.24201920T>G GRCh37
NC_000001.9:g.24074507T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374472.5:c.188A>C MANE Select ENSP00000363596.4:p.Gln63Pro
ENST00000374472.4:c.188A>C ENSP00000363596.4:p.Gln63Pro
NM_001841.2:c.188A>C NP_001832.1:p.Gln63Pro
XM_005245736.3:c.188A>C XP_005245793.1:p.Gln63Pro
XM_011540627.1:c.188A>C XP_011538929.1:p.Gln63Pro
XM_011540628.1:c.188A>C XP_011538930.1:p.Gln63Pro
XM_011540629.1:c.188A>C XP_011538931.1:p.Gln63Pro
XM_011540629.3:c.188A>C XP_011538931.1:p.Gln63Pro
XM_017000261.2:c.188A>C XP_016855750.1:p.Gln63Pro
NM_001841.3:c.188A>C MANE Select NP_001832.1:p.Gln63Pro