Canonical Allele Identifier: CA2483404343

Gene: CR2

Linked Data

• dbSNP Id: rs1657746038

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207453922del , CM000663.2:g.207453922del	GRCh38
NC_000001.10:g.207627267del , CM000663.1:g.207627267del	GRCh37
NC_000001.9:g.205693890del	NCBI36
NG_013006.1:g.4623del , LRG_348:g.4623del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699640.1:c.-385+827del	ENSP00000514493.1:n.-385+827del