Canonical Allele Identifier: CA344533946

Gene: CR2

Linked Data

• MyVariant Identifiers: chr1:g.207646229A>C (hg19) ; chr1:g.207472884A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207472884A>C , CM000663.2:g.207472884A>C	GRCh38
NC_000001.10:g.207646229A>C , CM000663.1:g.207646229A>C	GRCh37
NC_000001.9:g.205712852A>C	NCBI36
NG_013006.1:g.23585A>C , LRG_348:g.23585A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000699620.1:c.1314A>C	ENSP00000514480.1:p.Glu438Asp
ENST00000699621.1:c.1303A>C
ENST00000367057.8:c.1683A>C MANE Select	ENSP00000356024.3:p.Glu561Asp
ENST00000640301.1:c.133A>C	ENSP00000491608.1:n.133A>C
ENST00000367057.7:c.1683A>C	ENSP00000356024.3:p.Glu561Asp
ENST00000367058.7:c.1683A>C	ENSP00000356025.3:p.Glu561Asp
ENST00000367059.3:c.1683A>C	ENSP00000356026.3:p.Glu561Asp
NM_001006658.2:c.1683A>C , LRG_348t1:c.1683A>C	NP_001006659.1:p.Glu561Asp
NM_001877.4:c.1683A>C	NP_001868.2:p.Glu561Asp
XM_011509206.1:c.1314A>C	XP_011507508.1:p.Glu438Asp
XM_011509206.3:c.1314A>C	XP_011507508.1:p.Glu438Asp
NM_001006658.3:c.1683A>C MANE Select	NP_001006659.1:p.Glu561Asp
NM_001877.5:c.1683A>C	NP_001868.2:p.Glu561Asp