Canonical Allele Identifier: CA2483404602

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454374C= , CM000663.2:g.207454374C=	GRCh38
NC_000001.10:g.207627719C= , CM000663.1:g.207627719C=	GRCh37
NC_000001.9:g.205694342C=	NCBI36
NG_013006.1:g.5075C= , LRG_348:g.5075C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-487C=	ENSP00000514480.1:n.-487C=
ENST00000699640.1:c.-385+1279C=	ENSP00000514493.1:n.-385+1279C=
ENST00000367057.8:c.-45C= MANE Select	ENSP00000356024.3:n.-45C=
ENST00000367057.7:c.-45C=	ENSP00000356024.3:n.-45C=
ENST00000367058.7:c.-45C=	ENSP00000356025.3:n.-45C=
ENST00000367059.3:c.-45C=	ENSP00000356026.3:n.-45C=
NM_001006658.2:c.-45C= , LRG_348t1:c.-45C=	NP_001006659.1:n.-45C=
NM_001877.4:c.-45C=	NP_001868.2:n.-45C=
NM_001006658.3:c.-45C= MANE Select	NP_001006659.1:n.-45C=
NM_001877.5:c.-45C=	NP_001868.2:n.-45C=