Canonical Allele Identifier: CA1141940511

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207472877G= , CM000663.2:g.207472877G=	GRCh38
NC_000001.10:g.207646222G= , CM000663.1:g.207646222G=	GRCh37
NC_000001.9:g.205712845G=	NCBI36
NG_013006.1:g.23578G= , LRG_348:g.23578G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699620.1:c.1307G=	ENSP00000514480.1:p.Gly436=
ENST00000699621.1:c.1296G=
ENST00000367057.8:c.1676G= MANE Select	ENSP00000356024.3:p.Gly559=
ENST00000640301.1:c.126G=	ENSP00000491608.1:n.126G=
ENST00000367057.7:c.1676G=	ENSP00000356024.3:p.Gly559=
ENST00000367058.7:c.1676G=	ENSP00000356025.3:p.Gly559=
ENST00000367059.3:c.1676G=	ENSP00000356026.3:p.Gly559=
NM_001006658.2:c.1676G= , LRG_348t1:c.1676G=	NP_001006659.1:p.Gly559=
NM_001877.4:c.1676G=	NP_001868.2:p.Gly559=
XM_011509206.1:c.1307G=	XP_011507508.1:p.Gly436=
XM_011509206.3:c.1307G=	XP_011507508.1:p.Gly436=
NM_001006658.3:c.1676G= MANE Select	NP_001006659.1:p.Gly559=
NM_001877.5:c.1676G=	NP_001868.2:p.Gly559=