Canonical Allele Identifier: CA14473694
Gene:

Linked Data

ClinVar Variation Id: 1266799
ClinVar RCV Id: RCV001670468
dbSNP Id: rs4985754
gnomAD v2: 17-16875636-C-A
gnomAD v3: 17-16972322-C-A
gnomAD v4: 17-16972322-C-A
MyVariant Identifiers: chr17:g.16875636C>A (hg19) chr17:g.16972322C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16972322C>A , CM000679.2:g.16972322C>A GRCh38
NC_000017.10:g.16875636C>A , CM000679.1:g.16875636C>A GRCh37
NC_000017.9:g.16816361C>A NCBI36
NG_007281.1:g.4767G>T , LRG_120:g.4767G>T
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