Canonical Allele Identifier: CA2483404599

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454369A= , CM000663.2:g.207454369A=	GRCh38
NC_000001.10:g.207627714A= , CM000663.1:g.207627714A=	GRCh37
NC_000001.9:g.205694337A=	NCBI36
NG_013006.1:g.5070A= , LRG_348:g.5070A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699620.1:c.-492A=	ENSP00000514480.1:n.-492A=
ENST00000699640.1:c.-385+1274A=	ENSP00000514493.1:n.-385+1274A=
ENST00000367057.8:c.-50A= MANE Select	ENSP00000356024.3:n.-50A=
ENST00000367057.7:c.-50A=	ENSP00000356024.3:n.-50A=
ENST00000367058.7:c.-50A=	ENSP00000356025.3:n.-50A=
ENST00000367059.3:c.-50A=	ENSP00000356026.3:n.-50A=
NM_001006658.2:c.-50A= , LRG_348t1:c.-50A=	NP_001006659.1:n.-50A=
NM_001877.4:c.-50A=	NP_001868.2:n.-50A=
NM_001006658.3:c.-50A= MANE Select	NP_001006659.1:n.-50A=
NM_001877.5:c.-50A=	NP_001868.2:n.-50A=