Canonical Allele Identifier: CA1368478

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207468705C>G , CM000663.2:g.207468705C>G	GRCh38
NC_000001.10:g.207642050C>G , CM000663.1:g.207642050C>G	GRCh37
NC_000001.9:g.205708673C>G	NCBI36
NG_013006.1:g.19406C>G , LRG_348:g.19406C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.255C>G	ENSP00000514480.1:p.Pro85=
ENST00000699621.1:c.355C>G
ENST00000367057.8:c.624C>G MANE Select	ENSP00000356024.3:p.Pro208=
ENST00000367057.7:c.624C>G	ENSP00000356024.3:p.Pro208=
ENST00000367058.7:c.624C>G	ENSP00000356025.3:p.Pro208=
ENST00000367059.3:c.624C>G	ENSP00000356026.3:p.Pro208=
ENST00000485707.1:n.400C>G
NM_001006658.2:c.624C>G , LRG_348t1:c.624C>G	NP_001006659.1:p.Pro208=
NM_001877.4:c.624C>G	NP_001868.2:p.Pro208=
XM_011509206.1:c.255C>G	XP_011507508.1:p.Pro85=
XM_011509206.3:c.255C>G	XP_011507508.1:p.Pro85=
NM_001006658.3:c.624C>G MANE Select	NP_001006659.1:p.Pro208=
NM_001877.5:c.624C>G	NP_001868.2:p.Pro208=