Canonical Allele Identifier: CA2650261407
Gene: CR2 HGNC NCBI

Linked Data

gnomAD v4: 1-207454400-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454400C>A , CM000663.2:g.207454400C>A GRCh38
NC_000001.10:g.207627745C>A , CM000663.1:g.207627745C>A GRCh37
NC_000001.9:g.205694368C>A NCBI36
NG_013006.1:g.5101C>A , LRG_348:g.5101C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699620.1:c.-461C>A ENSP00000514480.1:n.-461C>A
ENST00000699640.1:c.-385+1305C>A ENSP00000514493.1:n.-385+1305C>A
ENST00000367057.8:c.-19C>A MANE Select ENSP00000356024.3:n.-19C>A
ENST00000367057.7:c.-19C>A ENSP00000356024.3:n.-19C>A
ENST00000367058.7:c.-19C>A ENSP00000356025.3:n.-19C>A
ENST00000367059.3:c.-19C>A ENSP00000356026.3:n.-19C>A
NM_001006658.2:c.-19C>A , LRG_348t1:c.-19C>A NP_001006659.1:n.-19C>A
NM_001877.4:c.-19C>A NP_001868.2:n.-19C>A
NM_001006658.3:c.-19C>A MANE Select NP_001006659.1:n.-19C>A
NM_001877.5:c.-19C>A NP_001868.2:n.-19C>A
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