Canonical Allele Identifier: CA2650261141
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454191_207454192insCCAGG , CM000663.2:g.207454191_207454192insCCAGG GRCh38
NC_000001.10:g.207627536_207627537insCCAGG , CM000663.1:g.207627536_207627537insCCAGG GRCh37
NC_000001.9:g.205694159_205694160insCCAGG NCBI36
NG_013006.1:g.4892_4893insCCAGG , LRG_348:g.4892_4893insCCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1096_-385+1097insCCAGG ENSP00000514493.1:n.-385+1096_-385+1097insCCAGG