Canonical Allele Identifier: CA730645868
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1465236825

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454297A>G , CM000663.2:g.207454297A>G GRCh38
NC_000001.10:g.207627642A>G , CM000663.1:g.207627642A>G GRCh37
NC_000001.9:g.205694265A>G NCBI36
NG_013006.1:g.4998A>G , LRG_348:g.4998A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1202A>G ENSP00000514493.1:n.-385+1202A>G
ENST00000367057.7:c.-122A>G ENSP00000356024.3:n.-122A>G
ENST00000367058.7:c.-122A>G ENSP00000356025.3:n.-122A>G
ENST00000367059.3:c.-122A>G ENSP00000356026.3:n.-122A>G