Canonical Allele Identifier: CA2483404374
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1657750153

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453985T>G , CM000663.2:g.207453985T>G GRCh38
NC_000001.10:g.207627330T>G , CM000663.1:g.207627330T>G GRCh37
NC_000001.9:g.205693953T>G NCBI36
NG_013006.1:g.4686T>G , LRG_348:g.4686T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+890T>G ENSP00000514493.1:n.-385+890T>G