Canonical Allele Identifier: CA423138946

Gene: CR2

Linked Data

• MyVariant Identifiers: chr1:g.207646223G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207472878G>A , CM000663.2:g.207472878G>A	GRCh38
NC_000001.10:g.207646223G>A , CM000663.1:g.207646223G>A	GRCh37
NC_000001.9:g.205712846G>A	NCBI36
NG_013006.1:g.23579G>A , LRG_348:g.23579G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000699620.1:c.1308G>A	ENSP00000514480.1:p.Gly436=
ENST00000699621.1:c.1297G>A
ENST00000367057.8:c.1677G>A MANE Select	ENSP00000356024.3:p.Gly559=
ENST00000640301.1:c.127G>A	ENSP00000491608.1:n.127G>A
ENST00000367057.7:c.1677G>A	ENSP00000356024.3:p.Gly559=
ENST00000367058.7:c.1677G>A	ENSP00000356025.3:p.Gly559=
ENST00000367059.3:c.1677G>A	ENSP00000356026.3:p.Gly559=
NM_001006658.2:c.1677G>A , LRG_348t1:c.1677G>A	NP_001006659.1:p.Gly559=
NM_001877.4:c.1677G>A	NP_001868.2:p.Gly559=
XM_011509206.1:c.1308G>A	XP_011507508.1:p.Gly436=
XM_011509206.3:c.1308G>A	XP_011507508.1:p.Gly436=
NM_001006658.3:c.1677G>A MANE Select	NP_001006659.1:p.Gly559=
NM_001877.5:c.1677G>A	NP_001868.2:p.Gly559=