Canonical Allele Identifier: CA2650261372
Gene: CR2 HGNC NCBI

Linked Data

gnomAD v4: 1-207454365-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454365C>A , CM000663.2:g.207454365C>A GRCh38
NC_000001.10:g.207627710C>A , CM000663.1:g.207627710C>A GRCh37
NC_000001.9:g.205694333C>A NCBI36
NG_013006.1:g.5066C>A , LRG_348:g.5066C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699620.1:c.-496C>A ENSP00000514480.1:n.-496C>A
ENST00000699640.1:c.-385+1270C>A ENSP00000514493.1:n.-385+1270C>A
ENST00000367057.8:c.-54C>A MANE Select ENSP00000356024.3:n.-54C>A
ENST00000367057.7:c.-54C>A ENSP00000356024.3:n.-54C>A
ENST00000367058.7:c.-54C>A ENSP00000356025.3:n.-54C>A
ENST00000367059.3:c.-54C>A ENSP00000356026.3:n.-54C>A
NM_001006658.2:c.-54C>A , LRG_348t1:c.-54C>A NP_001006659.1:n.-54C>A
NM_001877.4:c.-54C>A NP_001868.2:n.-54C>A
NM_001006658.3:c.-54C>A MANE Select NP_001006659.1:n.-54C>A
NM_001877.5:c.-54C>A NP_001868.2:n.-54C>A
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