Canonical Allele Identifier: CA2650261259
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454271_207454272del , CM000663.2:g.207454271_207454272del GRCh38
NC_000001.10:g.207627616_207627617del , CM000663.1:g.207627616_207627617del GRCh37
NC_000001.9:g.205694239_205694240del NCBI36
NG_013006.1:g.4972_4973del , LRG_348:g.4972_4973del

Transcript Alleles

HGVS Amino-acid change
ENST00000699640.1:c.-385+1176_-385+1177del ENSP00000514493.1:n.-385+1176_-385+1177de...
ENST00000367057.7:c.-148_-147del ENSP00000356024.3:n.-148_-147del
ENST00000367058.7:c.-148_-147del ENSP00000356025.3:n.-148_-147del
ENST00000367059.3:c.-148_-147del ENSP00000356026.3:n.-148_-147del