Canonical Allele Identifier: CA2483404471
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454170A= , CM000663.2:g.207454170A= GRCh38
NC_000001.10:g.207627515A= , CM000663.1:g.207627515A= GRCh37
NC_000001.9:g.205694138A= NCBI36
NG_013006.1:g.4871A= , LRG_348:g.4871A=

Transcript Alleles

HGVS Amino-acid change
ENST00000699640.1:c.-385+1075A= ENSP00000514493.1:n.-385+1075A=