Allele Registry

Canonical Allele Identifier: CA12274713

Gene: CNR1 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.88168233G>A

GRCh37 chr6:g.88877952G>A

Linked Data - Sequence & Population

gnomAD v2:

6:88877952 G / A

gnomAD v3:

6:88168233 G / A

gnomAD v4:

chr6-88168233-G-A

Joint Max Group AF 0.75409635 (EAS)

Genomes Max Group AF 0.75409635 (EAS)

Linked Data - NCBI & NCI

dbSNP:

2180619

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.88168233G>A , CM000668.2:g.88168233G>A	GRCh38
NC_000006.11:g.88877952G>A , CM000668.1:g.88877952G>A	GRCh37
NC_000006.10:g.88934671G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017010240.2:c.-1107C>T	XP_016865729.1:n.-1107C>T

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