Canonical Allele Identifier: CA10766008
Gene: CNR2 HGNC NCBI
COSMIC:
COSN6450328 (not active)
MyVariant.info:
GRCh38 chr1:g.23893573A>G
GRCh37 chr1:g.24220063A>G
gnomAD v2:
1:24220063 A / G
gnomAD v3:
1:23893573 A / G
gnomAD v4:
chr1-23893573-A-G
Joint Max Group AF 0.82358325 (AMR)
Genomes Max Group AF 0.82358325 (AMR)
dbSNP:
2501401
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23893573A>G , CM000663.2:g.23893573A>G GRCh38
NC_000001.10:g.24220063A>G , CM000663.1:g.24220063A>G GRCh37
NC_000001.9:g.24092650A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374472.5:c.-45-17911T>C MANE Select ENSP00000363596.4:n.-45-17911T>C
ENST00000374472.4:c.-45-17911T>C ENSP00000363596.4:n.-45-17911T>C
NM_001841.2:c.-45-17911T>C NP_001832.1:n.-45-17911T>C
NM_001841.3:c.-45-17911T>C MANE Select NP_001832.1:n.-45-17911T>C
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