Canonical Allele Identifier: CA1011643107
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1657751516
gnomAD v3: 1-207454021-A-G
gnomAD v4: 1-207454021-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454021A>G , CM000663.2:g.207454021A>G GRCh38
NC_000001.10:g.207627366A>G , CM000663.1:g.207627366A>G GRCh37
NC_000001.9:g.205693989A>G NCBI36
NG_013006.1:g.4722A>G , LRG_348:g.4722A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+926A>G ENSP00000514493.1:n.-385+926A>G
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