Canonical Allele Identifier: CA2483404552
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454300A= , CM000663.2:g.207454300A= GRCh38
NC_000001.10:g.207627645A= , CM000663.1:g.207627645A= GRCh37
NC_000001.9:g.205694268A= NCBI36
NG_013006.1:g.5001A= , LRG_348:g.5001A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1205A= ENSP00000514493.1:n.-385+1205A=
ENST00000367057.7:c.-119A= ENSP00000356024.3:n.-119A=
ENST00000367058.7:c.-119A= ENSP00000356025.3:n.-119A=
ENST00000367059.3:c.-119A= ENSP00000356026.3:n.-119A=
NM_001006658.2:c.-119A= , LRG_348t1:c.-119A= NP_001006659.1:n.-119A=
NM_001877.4:c.-119A= NP_001868.2:n.-119A=