Canonical Allele Identifier: CA1147434769
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454087T= , CM000663.2:g.207454087T= GRCh38
NC_000001.10:g.207627432T= , CM000663.1:g.207627432T= GRCh37
NC_000001.9:g.205694055T= NCBI36
NG_013006.1:g.4788T= , LRG_348:g.4788T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+992T= ENSP00000514493.1:n.-385+992T=