Canonical Allele Identifier: CA2483404589

Gene: CR2

Linked Data

• dbSNP Id: rs1657772602
• gnomAD v4: 1-207454359-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454359G>C , CM000663.2:g.207454359G>C	GRCh38
NC_000001.10:g.207627704G>C , CM000663.1:g.207627704G>C	GRCh37
NC_000001.9:g.205694327G>C	NCBI36
NG_013006.1:g.5060G>C , LRG_348:g.5060G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-502G>C	ENSP00000514480.1:n.-502G>C
ENST00000699640.1:c.-385+1264G>C	ENSP00000514493.1:n.-385+1264G>C
ENST00000367057.8:c.-60G>C MANE Select	ENSP00000356024.3:n.-60G>C
ENST00000367057.7:c.-60G>C	ENSP00000356024.3:n.-60G>C
ENST00000367058.7:c.-60G>C	ENSP00000356025.3:n.-60G>C
ENST00000367059.3:c.-60G>C	ENSP00000356026.3:n.-60G>C
NM_001006658.2:c.-60G>C , LRG_348t1:c.-60G>C	NP_001006659.1:n.-60G>C
NM_001877.4:c.-60G>C	NP_001868.2:n.-60G>C
NM_001006658.3:c.-60G>C MANE Select	NP_001006659.1:n.-60G>C
NM_001877.5:c.-60G>C	NP_001868.2:n.-60G>C