Canonical Allele Identifier: CA686794
Gene: CNR2 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.23875153G>A
GRCh37 chr1:g.24201643G>A
gnomAD v2:
1:24201643 G / A
gnomAD v3:
1:23875153 G / A
gnomAD v4:
chr1-23875153-G-A
Joint Max Group AF 0.75503668 (AFR)
Genomes Max Group AF 0.74901946 (AFR)
Exomes Max Group AF 0.75767009 (AFR)
dbSNP:
2501431
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23875153G>A , CM000663.2:g.23875153G>A GRCh38
NC_000001.10:g.24201643G>A , CM000663.1:g.24201643G>A GRCh37
NC_000001.9:g.24074230G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374472.5:c.465C>T MANE Select ENSP00000363596.4:p.Gly155=
ENST00000374472.4:c.465C>T ENSP00000363596.4:p.Gly155=
NM_001841.2:c.465C>T NP_001832.1:p.Gly155=
XM_005245736.3:c.465C>T XP_005245793.1:p.Gly155=
XM_011540627.1:c.465C>T XP_011538929.1:p.Gly155=
XM_011540628.1:c.465C>T XP_011538930.1:p.Gly155=
XM_011540629.1:c.465C>T XP_011538931.1:p.Gly155=
XM_011540629.3:c.465C>T XP_011538931.1:p.Gly155=
XM_017000261.2:c.465C>T XP_016855750.1:p.Gly155=
NM_001841.3:c.465C>T MANE Select NP_001832.1:p.Gly155=
Search 100 bp 5'
Search 100 bp 3'