Canonical Allele Identifier: CA730645791
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1356903768
gnomAD v3: 1-207454170-A-T
gnomAD v4: 1-207454170-A-T
MyVariant Identifiers: chr1:g.207627515A>T (hg19) chr1:g.207454170A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454170A>T , CM000663.2:g.207454170A>T GRCh38
NC_000001.10:g.207627515A>T , CM000663.1:g.207627515A>T GRCh37
NC_000001.9:g.205694138A>T NCBI36
NG_013006.1:g.4871A>T , LRG_348:g.4871A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1075A>T ENSP00000514493.1:n.-385+1075A>T
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