Canonical Allele Identifier: CA1368862

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207473572A>G , CM000663.2:g.207473572A>G	GRCh38
NC_000001.10:g.207646917A>G , CM000663.1:g.207646917A>G	GRCh37
NC_000001.9:g.205713540A>G	NCBI36
NG_013006.1:g.24273A>G , LRG_348:g.24273A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.1610-229A>G	ENSP00000514480.1:n.1610-229A>G
ENST00000699621.1:c.1599-229A>G
ENST00000367057.8:c.2006A>G MANE Select	ENSP00000356024.3:p.His669Arg
ENST00000367057.7:c.2006A>G	ENSP00000356024.3:p.His669Arg
ENST00000367058.7:c.1979-229A>G	ENSP00000356025.3:n.1979-229A>G
ENST00000367059.3:c.1979-229A>G	ENSP00000356026.3:n.1979-229A>G
NM_001006658.2:c.2006A>G , LRG_348t1:c.2006A>G	NP_001006659.1:p.His669Arg
NM_001877.4:c.1979-229A>G	NP_001868.2:n.1979-229A>G
XM_011509206.1:c.1637A>G	XP_011507508.1:p.His546Arg
XM_011509206.3:c.1637A>G	XP_011507508.1:p.His546Arg
NM_001006658.3:c.2006A>G MANE Select	NP_001006659.1:p.His669Arg
NM_001877.5:c.1979-229A>G	NP_001868.2:n.1979-229A>G