Canonical Allele Identifier: CA2483404429
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454096_207454100delinsCAAGT , CM000663.2:g.207454096_207454100delinsCAAGT GRCh38
NC_000001.10:g.207627441_207627445delinsCAAGT , CM000663.1:g.207627441_207627445delinsCAAGT GRCh37
NC_000001.9:g.205694064_205694068delinsCAAGT NCBI36
NG_013006.1:g.4797_4801delinsCAAGT , LRG_348:g.4797_4801delinsCAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1001_-385+1005delinsCAAGT ENSP00000514493.1:n.-385+1001_-385+1005delinsCAAGT