Canonical Allele Identifier: CA1143717407

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454400C= , CM000663.2:g.207454400C=	GRCh38
NC_000001.10:g.207627745C= , CM000663.1:g.207627745C=	GRCh37
NC_000001.9:g.205694368C=	NCBI36
NG_013006.1:g.5101C= , LRG_348:g.5101C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-461C=	ENSP00000514480.1:n.-461C=
ENST00000699640.1:c.-385+1305C=	ENSP00000514493.1:n.-385+1305C=
ENST00000367057.8:c.-19C= MANE Select	ENSP00000356024.3:n.-19C=
ENST00000367057.7:c.-19C=	ENSP00000356024.3:n.-19C=
ENST00000367058.7:c.-19C=	ENSP00000356025.3:n.-19C=
ENST00000367059.3:c.-19C=	ENSP00000356026.3:n.-19C=
NM_001006658.2:c.-19C= , LRG_348t1:c.-19C=	NP_001006659.1:n.-19C=
NM_001877.4:c.-19C=	NP_001868.2:n.-19C=
NM_001006658.3:c.-19C= MANE Select	NP_001006659.1:n.-19C=
NM_001877.5:c.-19C=	NP_001868.2:n.-19C=