Canonical Allele Identifier: CA1368622

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207469956G>A , CM000663.2:g.207469956G>A	GRCh38
NC_000001.10:g.207643301G>A , CM000663.1:g.207643301G>A	GRCh37
NC_000001.9:g.205709924G>A	NCBI36
NG_013006.1:g.20657G>A , LRG_348:g.20657G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.710G>A	ENSP00000514480.1:p.Arg237Gln
ENST00000699621.1:c.699G>A
ENST00000367057.8:c.1079G>A MANE Select	ENSP00000356024.3:p.Arg360Gln
ENST00000367057.7:c.1079G>A	ENSP00000356024.3:p.Arg360Gln
ENST00000367058.7:c.1079G>A	ENSP00000356025.3:p.Arg360Gln
ENST00000367059.3:c.1079G>A	ENSP00000356026.3:p.Arg360Gln
NM_001006658.2:c.1079G>A , LRG_348t1:c.1079G>A	NP_001006659.1:p.Arg360Gln
NM_001877.4:c.1079G>A	NP_001868.2:p.Arg360Gln
XM_011509206.1:c.710G>A	XP_011507508.1:p.Arg237Gln
XM_011509206.3:c.710G>A	XP_011507508.1:p.Arg237Gln
NM_001006658.3:c.1079G>A MANE Select	NP_001006659.1:p.Arg360Gln
NM_001877.5:c.1079G>A	NP_001868.2:p.Arg360Gln