Canonical Allele Identifier: CA2483404618

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454392T= , CM000663.2:g.207454392T=	GRCh38
NC_000001.10:g.207627737T= , CM000663.1:g.207627737T=	GRCh37
NC_000001.9:g.205694360T=	NCBI36
NG_013006.1:g.5093T= , LRG_348:g.5093T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-469T=	ENSP00000514480.1:n.-469T=
ENST00000699640.1:c.-385+1297T=	ENSP00000514493.1:n.-385+1297T=
ENST00000367057.8:c.-27T= MANE Select	ENSP00000356024.3:n.-27T=
ENST00000367057.7:c.-27T=	ENSP00000356024.3:n.-27T=
ENST00000367058.7:c.-27T=	ENSP00000356025.3:n.-27T=
ENST00000367059.3:c.-27T=	ENSP00000356026.3:n.-27T=
NM_001006658.2:c.-27T= , LRG_348t1:c.-27T=	NP_001006659.1:n.-27T=
NM_001877.4:c.-27T=	NP_001868.2:n.-27T=
NM_001006658.3:c.-27T= MANE Select	NP_001006659.1:n.-27T=
NM_001877.5:c.-27T=	NP_001868.2:n.-27T=