Canonical Allele Identifier: CA1369159

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207480019A>G , CM000663.2:g.207480019A>G	GRCh38
NC_000001.10:g.207653364A>G , CM000663.1:g.207653364A>G	GRCh37
NC_000001.9:g.205719987A>G	NCBI36
NG_013006.1:g.30720A>G , LRG_348:g.30720A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.2608A>G	ENSP00000514480.1:p.Ile870Val
ENST00000699621.1:c.2573A>G
ENST00000367057.8:c.3154A>G MANE Select	ENSP00000356024.3:p.Ile1052Val
ENST00000367057.7:c.3154A>G	ENSP00000356024.3:p.Ile1052Val
ENST00000367058.7:c.2977A>G	ENSP00000356025.3:p.Ile993Val
ENST00000367059.3:c.2791A>G	ENSP00000356026.3:p.Ile931Val
NM_001006658.2:c.3154A>G , LRG_348t1:c.3154A>G	NP_001006659.1:p.Ile1052Val
NM_001877.4:c.2977A>G	NP_001868.2:p.Ile993Val
XM_011509206.1:c.2785A>G	XP_011507508.1:p.Ile929Val
XM_011509206.3:c.2785A>G	XP_011507508.1:p.Ile929Val
NM_001006658.3:c.3154A>G MANE Select	NP_001006659.1:p.Ile1052Val
NM_001877.5:c.2977A>G	NP_001868.2:p.Ile993Val