Canonical Allele Identifier: CA2483404547
Gene: CR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454286G= , CM000663.2:g.207454286G= GRCh38
NC_000001.10:g.207627631G= , CM000663.1:g.207627631G= GRCh37
NC_000001.9:g.205694254G= NCBI36
NG_013006.1:g.4987G= , LRG_348:g.4987G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1191G= ENSP00000514493.1:n.-385+1191G=
ENST00000367057.7:c.-133G= ENSP00000356024.3:n.-133G=
ENST00000367058.7:c.-133G= ENSP00000356025.3:n.-133G=
ENST00000367059.3:c.-133G= ENSP00000356026.3:n.-133G=
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