Canonical Allele Identifier: CA2483404352
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453944G= , CM000663.2:g.207453944G= GRCh38
NC_000001.10:g.207627289G= , CM000663.1:g.207627289G= GRCh37
NC_000001.9:g.205693912G= NCBI36
NG_013006.1:g.4645G= , LRG_348:g.4645G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+849G= ENSP00000514493.1:n.-385+849G=