Canonical Allele Identifier: CA2650261327
Gene: CR2 HGNC NCBI

Linked Data

gnomAD v4: 1-207454328-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454328A>G , CM000663.2:g.207454328A>G GRCh38
NC_000001.10:g.207627673A>G , CM000663.1:g.207627673A>G GRCh37
NC_000001.9:g.205694296A>G NCBI36
NG_013006.1:g.5029A>G , LRG_348:g.5029A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1233A>G ENSP00000514493.1:n.-385+1233A>G
ENST00000367057.8:c.-91A>G MANE Select ENSP00000356024.3:n.-91A>G
ENST00000367057.7:c.-91A>G ENSP00000356024.3:n.-91A>G
ENST00000367058.7:c.-91A>G ENSP00000356025.3:n.-91A>G
ENST00000367059.3:c.-91A>G ENSP00000356026.3:n.-91A>G
NM_001006658.2:c.-91A>G , LRG_348t1:c.-91A>G NP_001006659.1:n.-91A>G
NM_001877.4:c.-91A>G NP_001868.2:n.-91A>G
NM_001006658.3:c.-91A>G MANE Select NP_001006659.1:n.-91A>G
NM_001877.5:c.-91A>G NP_001868.2:n.-91A>G
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