Canonical Allele Identifier: CA1011643150
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1657762612
gnomAD v3: 1-207454147-C-G
gnomAD v4: 1-207454147-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454147C>G , CM000663.2:g.207454147C>G GRCh38
NC_000001.10:g.207627492C>G , CM000663.1:g.207627492C>G GRCh37
NC_000001.9:g.205694115C>G NCBI36
NG_013006.1:g.4848C>G , LRG_348:g.4848C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1052C>G ENSP00000514493.1:n.-385+1052C>G
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