Canonical Allele Identifier: CA2483404324
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453855_207453859delinsTAAAG , CM000663.2:g.207453855_207453859delinsTAAAG GRCh38
NC_000001.10:g.207627200_207627204delinsTAAAG , CM000663.1:g.207627200_207627204delinsTAAAG GRCh37
NC_000001.9:g.205693823_205693827delinsTAAAG NCBI36
NG_013006.1:g.4556_4560delinsTAAAG , LRG_348:g.4556_4560delinsTAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+760_-385+764delinsTAAAG ENSP00000514493.1:n.-385+760_-385+764delinsTAAAG