Canonical Allele Identifier: CA528606454

Gene: CR2

Linked Data

• dbSNP Id: rs1445427078
• gnomAD v2: 1-207627736-A-G
• gnomAD v4: 1-207454391-A-G
• MyVariant Identifiers: chr1:g.207627736A>G (hg19) ; chr1:g.207454391A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454391A>G , CM000663.2:g.207454391A>G	GRCh38
NC_000001.10:g.207627736A>G , CM000663.1:g.207627736A>G	GRCh37
NC_000001.9:g.205694359A>G	NCBI36
NG_013006.1:g.5092A>G , LRG_348:g.5092A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-470A>G	ENSP00000514480.1:n.-470A>G
ENST00000699640.1:c.-385+1296A>G	ENSP00000514493.1:n.-385+1296A>G
ENST00000367057.8:c.-28A>G MANE Select	ENSP00000356024.3:n.-28A>G
ENST00000367057.7:c.-28A>G	ENSP00000356024.3:n.-28A>G
ENST00000367058.7:c.-28A>G	ENSP00000356025.3:n.-28A>G
ENST00000367059.3:c.-28A>G	ENSP00000356026.3:n.-28A>G
NM_001006658.2:c.-28A>G , LRG_348t1:c.-28A>G	NP_001006659.1:n.-28A>G
NM_001877.4:c.-28A>G	NP_001868.2:n.-28A>G
NM_001006658.3:c.-28A>G MANE Select	NP_001006659.1:n.-28A>G
NM_001877.5:c.-28A>G	NP_001868.2:n.-28A>G