Canonical Allele Identifier: CA123811
Gene:

Linked Data

ClinVar Variation Id: 14207
ClinVar RCV Id: RCV000015271 RCV000015272 RCV000015273 RCV000015274 RCV003974826
dbSNP Id: rs1024611 rs2151345376 rs2151345377 rs2151345381
gnomAD v2: 17-32579788-A-G
gnomAD v3: 17-34252769-A-G
gnomAD v4: 17-34252769-A-G
MyVariant Identifiers: chr17:g.32579788A>G (hg19) chr17:g.34252769A>G (hg38)
PubMed: PMID:11500196 PMID:15466648 PMID:16352737 PMID:16596675 PMID:18940815
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34252769A>G , CM000679.2:g.34252769A>G GRCh38
NC_000017.10:g.32579788A>G , CM000679.1:g.32579788A>G GRCh37
NC_000017.9:g.29603901A>G NCBI36
NG_012123.1:g.2493A>G
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