Canonical Allele Identifier: CA2483404331
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453877T= , CM000663.2:g.207453877T= GRCh38
NC_000001.10:g.207627222T= , CM000663.1:g.207627222T= GRCh37
NC_000001.9:g.205693845T= NCBI36
NG_013006.1:g.4578T= , LRG_348:g.4578T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+782T= ENSP00000514493.1:n.-385+782T=