Canonical Allele Identifier: CA2483404632

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454413C= , CM000663.2:g.207454413C=	GRCh38
NC_000001.10:g.207627758C= , CM000663.1:g.207627758C=	GRCh37
NC_000001.9:g.205694381C=	NCBI36
NG_013006.1:g.5114C= , LRG_348:g.5114C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-448C=	ENSP00000514480.1:n.-448C=
ENST00000699640.1:c.-385+1318C=	ENSP00000514493.1:n.-385+1318C=
ENST00000367057.8:c.-6C= MANE Select	ENSP00000356024.3:n.-6C=
ENST00000367057.7:c.-6C=	ENSP00000356024.3:n.-6C=
ENST00000367058.7:c.-6C=	ENSP00000356025.3:n.-6C=
ENST00000367059.3:c.-6C=	ENSP00000356026.3:n.-6C=
NM_001006658.2:c.-6C= , LRG_348t1:c.-6C=	NP_001006659.1:n.-6C=
NM_001877.4:c.-6C=	NP_001868.2:n.-6C=
NM_001006658.3:c.-6C= MANE Select	NP_001006659.1:n.-6C=
NM_001877.5:c.-6C=	NP_001868.2:n.-6C=