Canonical Allele Identifier: CA2650261277
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454286_207454296del , CM000663.2:g.207454286_207454296del GRCh38
NC_000001.10:g.207627631_207627641del , CM000663.1:g.207627631_207627641del GRCh37
NC_000001.9:g.205694254_205694264del NCBI36
NG_013006.1:g.4987_4997del , LRG_348:g.4987_4997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1191_-385+1201del ENSP00000514493.1:n.-385+1191_-385+1201del
ENST00000367057.7:c.-133_-123del ENSP00000356024.3:n.-133_-123del
ENST00000367058.7:c.-133_-123del ENSP00000356025.3:n.-133_-123del
ENST00000367059.3:c.-133_-123del ENSP00000356026.3:n.-133_-123del