Canonical Allele Identifier: CA2483404591
Gene: CR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454361G= , CM000663.2:g.207454361G= GRCh38
NC_000001.10:g.207627706G= , CM000663.1:g.207627706G= GRCh37
NC_000001.9:g.205694329G= NCBI36
NG_013006.1:g.5062G= , LRG_348:g.5062G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699620.1:c.-500G= ENSP00000514480.1:n.-500G=
ENST00000699640.1:c.-385+1266G= ENSP00000514493.1:n.-385+1266G=
ENST00000367057.8:c.-58G= MANE Select ENSP00000356024.3:n.-58G=
ENST00000367057.7:c.-58G= ENSP00000356024.3:n.-58G=
ENST00000367058.7:c.-58G= ENSP00000356025.3:n.-58G=
ENST00000367059.3:c.-58G= ENSP00000356026.3:n.-58G=
NM_001006658.2:c.-58G= , LRG_348t1:c.-58G= NP_001006659.1:n.-58G=
NM_001877.4:c.-58G= NP_001868.2:n.-58G=
NM_001006658.3:c.-58G= MANE Select NP_001006659.1:n.-58G=
NM_001877.5:c.-58G= NP_001868.2:n.-58G=