Canonical Allele Identifier: CA2483404571

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454334T= , CM000663.2:g.207454334T=	GRCh38
NC_000001.10:g.207627679T= , CM000663.1:g.207627679T=	GRCh37
NC_000001.9:g.205694302T=	NCBI36
NG_013006.1:g.5035T= , LRG_348:g.5035T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699640.1:c.-385+1239T=	ENSP00000514493.1:n.-385+1239T=
ENST00000367057.8:c.-85T= MANE Select	ENSP00000356024.3:n.-85T=
ENST00000367057.7:c.-85T=	ENSP00000356024.3:n.-85T=
ENST00000367058.7:c.-85T=	ENSP00000356025.3:n.-85T=
ENST00000367059.3:c.-85T=	ENSP00000356026.3:n.-85T=
NM_001006658.2:c.-85T= , LRG_348t1:c.-85T=	NP_001006659.1:n.-85T=
NM_001877.4:c.-85T=	NP_001868.2:n.-85T=
NM_001006658.3:c.-85T= MANE Select	NP_001006659.1:n.-85T=
NM_001877.5:c.-85T=	NP_001868.2:n.-85T=