Canonical Allele Identifier: CA2483404478
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1657764211

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1085A>T ENSP00000514493.1:n.-385+1085A>T