Canonical Allele Identifier: CA1368944

Gene: CR2

Linked Data

• ClinVar Variation Id: 473097
• ClinVar RCV Id: RCV000542242 ; RCV000757139
• dbSNP Id: rs151093663
• ExAC: 1:207647643 G / A
• gnomAD v2: 1-207647643-G-A
• gnomAD v3: 1-207474298-G-A
• gnomAD v4: 1-207474298-G-A
• MyVariant Identifiers: chr1:g.207647643G>A (hg19) ; chr1:g.207474298G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207474298G>A , CM000663.2:g.207474298G>A	GRCh38
NC_000001.10:g.207647643G>A , CM000663.1:g.207647643G>A	GRCh37
NC_000001.9:g.205714266G>A	NCBI36
NG_013006.1:g.24999G>A , LRG_348:g.24999G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.1752G>A	ENSP00000514480.1:p.Trp584Ter
ENST00000699621.1:c.1741G>A
ENST00000367057.8:c.2298G>A MANE Select	ENSP00000356024.3:p.Trp766Ter
ENST00000367057.7:c.2298G>A	ENSP00000356024.3:p.Trp766Ter
ENST00000367058.7:c.2121G>A	ENSP00000356025.3:p.Trp707Ter
ENST00000367059.3:c.2121G>A	ENSP00000356026.3:p.Trp707Ter
NM_001006658.2:c.2298G>A , LRG_348t1:c.2298G>A	NP_001006659.1:p.Trp766Ter
NM_001877.4:c.2121G>A	NP_001868.2:p.Trp707Ter
XM_011509206.1:c.1929G>A	XP_011507508.1:p.Trp643Ter
XM_011509206.3:c.1929G>A	XP_011507508.1:p.Trp643Ter
NM_001006658.3:c.2298G>A MANE Select	NP_001006659.1:p.Trp766Ter
NM_001877.5:c.2121G>A	NP_001868.2:p.Trp707Ter