Canonical Allele Identifier: CA2483404532
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454251C= , CM000663.2:g.207454251C= GRCh38
NC_000001.10:g.207627596C= , CM000663.1:g.207627596C= GRCh37
NC_000001.9:g.205694219C= NCBI36
NG_013006.1:g.4952C= , LRG_348:g.4952C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1156C= ENSP00000514493.1:n.-385+1156C=
ENST00000367057.7:c.-168C= ENSP00000356024.3:n.-168C=
ENST00000367058.7:c.-168C= ENSP00000356025.3:n.-168C=
ENST00000367059.3:c.-168C= ENSP00000356026.3:n.-168C=