Canonical Allele Identifier: CA2483404333
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1572941843

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453879C>G , CM000663.2:g.207453879C>G GRCh38
NC_000001.10:g.207627224C>G , CM000663.1:g.207627224C>G GRCh37
NC_000001.9:g.205693847C>G NCBI36
NG_013006.1:g.4580C>G , LRG_348:g.4580C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+784C>G ENSP00000514493.1:n.-385+784C>G