Canonical Allele Identifier: CA11915809
Gene:

Linked Data

ClinVar Variation Id: 225785
ClinVar RCV Id: RCV002515605
dbSNP Id: rs2736108
gnomAD v2: 5-1297488-C-T
gnomAD v3: 5-1297373-C-T
gnomAD v4: 5-1297373-C-T
MyVariant Identifiers: chr5:g.1297488C>T (hg19) chr5:g.1297373C>T (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1297373C>T , CM000667.2:g.1297373C>T GRCh38
NC_000005.9:g.1297488C>T , CM000667.1:g.1297488C>T GRCh37
NC_000005.8:g.1350488C>T NCBI36
NG_009265.1:g.2675G>A , LRG_343:g.2675G>A
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