Canonical Allele Identifier: CA344529391

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207470064A>G , CM000663.2:g.207470064A>G	GRCh38
NC_000001.10:g.207643409A>G , CM000663.1:g.207643409A>G	GRCh37
NC_000001.9:g.205710032A>G	NCBI36
NG_013006.1:g.20765A>G , LRG_348:g.20765A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.818A>G	ENSP00000514480.1:p.Gln273Arg
ENST00000699621.1:c.807A>G
ENST00000367057.8:c.1187A>G MANE Select	ENSP00000356024.3:p.Gln396Arg
ENST00000367057.7:c.1187A>G	ENSP00000356024.3:p.Gln396Arg
ENST00000367058.7:c.1187A>G	ENSP00000356025.3:p.Gln396Arg
ENST00000367059.3:c.1187A>G	ENSP00000356026.3:p.Gln396Arg
NM_001006658.2:c.1187A>G , LRG_348t1:c.1187A>G	NP_001006659.1:p.Gln396Arg
NM_001877.4:c.1187A>G	NP_001868.2:p.Gln396Arg
XM_011509206.1:c.818A>G	XP_011507508.1:p.Gln273Arg
XM_011509206.3:c.818A>G	XP_011507508.1:p.Gln273Arg
NM_001006658.3:c.1187A>G MANE Select	NP_001006659.1:p.Gln396Arg
NM_001877.5:c.1187A>G	NP_001868.2:p.Gln396Arg