Canonical Allele Identifier: CA2650261186
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454214_207454217del , CM000663.2:g.207454214_207454217del GRCh38
NC_000001.10:g.207627559_207627562del , CM000663.1:g.207627559_207627562del GRCh37
NC_000001.9:g.205694182_205694185del NCBI36
NG_013006.1:g.4915_4918del , LRG_348:g.4915_4918del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1119_-385+1122del ENSP00000514493.1:n.-385+1119_-385+1122del