Canonical Allele Identifier: CA730645603
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1340255949
gnomAD v3: 1-207453877-T-A
gnomAD v4: 1-207453877-T-A
MyVariant Identifiers: chr1:g.207627222T>A (hg19) chr1:g.207453877T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453877T>A , CM000663.2:g.207453877T>A GRCh38
NC_000001.10:g.207627222T>A , CM000663.1:g.207627222T>A GRCh37
NC_000001.9:g.205693845T>A NCBI36
NG_013006.1:g.4578T>A , LRG_348:g.4578T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+782T>A ENSP00000514493.1:n.-385+782T>A
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