Canonical Allele Identifier: CA19297807

Gene: CNR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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