Canonical Allele Identifier: CA1369018

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207475149T>C , CM000663.2:g.207475149T>C	GRCh38
NC_000001.10:g.207648494T>C , CM000663.1:g.207648494T>C	GRCh37
NC_000001.9:g.205715117T>C	NCBI36
NG_013006.1:g.25850T>C , LRG_348:g.25850T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.2103T>C	ENSP00000514480.1:p.Gly701=
ENST00000699621.1:c.2092T>C
ENST00000367057.8:c.2649T>C MANE Select	ENSP00000356024.3:p.Gly883=
ENST00000367057.7:c.2649T>C	ENSP00000356024.3:p.Gly883=
ENST00000367058.7:c.2472T>C	ENSP00000356025.3:p.Gly824=
ENST00000367059.3:c.2472T>C	ENSP00000356026.3:p.Gly824=
NM_001006658.2:c.2649T>C , LRG_348t1:c.2649T>C	NP_001006659.1:p.Gly883=
NM_001877.4:c.2472T>C	NP_001868.2:p.Gly824=
XM_011509206.1:c.2280T>C	XP_011507508.1:p.Gly760=
XM_011509206.3:c.2280T>C	XP_011507508.1:p.Gly760=
NM_001006658.3:c.2649T>C MANE Select	NP_001006659.1:p.Gly883=
NM_001877.5:c.2472T>C	NP_001868.2:p.Gly824=