Canonical Allele Identifier: CA2483404329
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453865A= , CM000663.2:g.207453865A= GRCh38
NC_000001.10:g.207627210A= , CM000663.1:g.207627210A= GRCh37
NC_000001.9:g.205693833A= NCBI36
NG_013006.1:g.4566A= , LRG_348:g.4566A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+770A= ENSP00000514493.1:n.-385+770A=