Canonical Allele Identifier: CA2650261318
Gene: CR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454320T>A , CM000663.2:g.207454320T>A GRCh38
NC_000001.10:g.207627665T>A , CM000663.1:g.207627665T>A GRCh37
NC_000001.9:g.205694288T>A NCBI36
NG_013006.1:g.5021T>A , LRG_348:g.5021T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1225T>A ENSP00000514493.1:n.-385+1225T>A
ENST00000367057.7:c.-99T>A ENSP00000356024.3:n.-99T>A
ENST00000367058.7:c.-99T>A ENSP00000356025.3:n.-99T>A
ENST00000367059.3:c.-99T>A ENSP00000356026.3:n.-99T>A
NM_001006658.2:c.-99T>A , LRG_348t1:c.-99T>A NP_001006659.1:n.-99T>A
NM_001877.4:c.-99T>A NP_001868.2:n.-99T>A