Canonical Allele Identifier: CA2483404525
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454246_207454247delinsGC , CM000663.2:g.207454246_207454247delinsGC GRCh38
NC_000001.10:g.207627591_207627592delinsGC , CM000663.1:g.207627591_207627592delinsGC GRCh37
NC_000001.9:g.205694214_205694215delinsGC NCBI36
NG_013006.1:g.4947_4948delinsGC , LRG_348:g.4947_4948delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1151_-385+1152delinsGC ENSP00000514493.1:n.-385+1151_-385+1152delinsGC
ENST00000367057.7:c.-173_-172delinsGC ENSP00000356024.3:n.-173_-172delinsGC
ENST00000367058.7:c.-173_-172delinsGC ENSP00000356025.3:n.-173_-172delinsGC
ENST00000367059.3:c.-173_-172delinsGC ENSP00000356026.3:n.-173_-172delinsGC