Canonical Allele Identifier: CA2483404477
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454180A= , CM000663.2:g.207454180A= GRCh38
NC_000001.10:g.207627525A= , CM000663.1:g.207627525A= GRCh37
NC_000001.9:g.205694148A= NCBI36
NG_013006.1:g.4881A= , LRG_348:g.4881A=

Transcript Alleles

HGVS Amino-acid change
ENST00000699640.1:c.-385+1085A= ENSP00000514493.1:n.-385+1085A=