Canonical Allele Identifier: CA1143703517

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454399G= , CM000663.2:g.207454399G=	GRCh38
NC_000001.10:g.207627744G= , CM000663.1:g.207627744G=	GRCh37
NC_000001.9:g.205694367G=	NCBI36
NG_013006.1:g.5100G= , LRG_348:g.5100G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-462G=	ENSP00000514480.1:n.-462G=
ENST00000699640.1:c.-385+1304G=	ENSP00000514493.1:n.-385+1304G=
ENST00000367057.8:c.-20G= MANE Select	ENSP00000356024.3:n.-20G=
ENST00000367057.7:c.-20G=	ENSP00000356024.3:n.-20G=
ENST00000367058.7:c.-20G=	ENSP00000356025.3:n.-20G=
ENST00000367059.3:c.-20G=	ENSP00000356026.3:n.-20G=
NM_001006658.2:c.-20G= , LRG_348t1:c.-20G=	NP_001006659.1:n.-20G=
NM_001877.4:c.-20G=	NP_001868.2:n.-20G=
NM_001006658.3:c.-20G= MANE Select	NP_001006659.1:n.-20G=
NM_001877.5:c.-20G=	NP_001868.2:n.-20G=