Canonical Allele Identifier: CA730645630
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1353877536
gnomAD v3: 1-207453934-T-A
gnomAD v4: 1-207453934-T-A
MyVariant Identifiers: chr1:g.207627279T>A (hg19) chr1:g.207453934T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453934T>A , CM000663.2:g.207453934T>A GRCh38
NC_000001.10:g.207627279T>A , CM000663.1:g.207627279T>A GRCh37
NC_000001.9:g.205693902T>A NCBI36
NG_013006.1:g.4635T>A , LRG_348:g.4635T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+839T>A ENSP00000514493.1:n.-385+839T>A
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