Canonical Allele Identifier: CA2483404613

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454389G= , CM000663.2:g.207454389G=	GRCh38
NC_000001.10:g.207627734G= , CM000663.1:g.207627734G=	GRCh37
NC_000001.9:g.205694357G=	NCBI36
NG_013006.1:g.5090G= , LRG_348:g.5090G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-472G=	ENSP00000514480.1:n.-472G=
ENST00000699640.1:c.-385+1294G=	ENSP00000514493.1:n.-385+1294G=
ENST00000367057.8:c.-30G= MANE Select	ENSP00000356024.3:n.-30G=
ENST00000367057.7:c.-30G=	ENSP00000356024.3:n.-30G=
ENST00000367058.7:c.-30G=	ENSP00000356025.3:n.-30G=
ENST00000367059.3:c.-30G=	ENSP00000356026.3:n.-30G=
NM_001006658.2:c.-30G= , LRG_348t1:c.-30G=	NP_001006659.1:n.-30G=
NM_001877.4:c.-30G=	NP_001868.2:n.-30G=
NM_001006658.3:c.-30G= MANE Select	NP_001006659.1:n.-30G=
NM_001877.5:c.-30G=	NP_001868.2:n.-30G=