ClinGen Allele Registry
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Canonical Allele Identifier:
CA289534249
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.34266955G>C
GRCh37
chr17:g.32593974G>C
Linked Data - Sequence & Population
gnomAD v3:
17:34266955 G / C
gnomAD v4:
chr17-34266955-G-C
Linked Data - NCBI & NCI
dbSNP:
3091316
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.34266955G>C , CM000679.2:g.34266955G>C
GRCh38
NC_000017.10:g.32593974G>C , CM000679.1:g.32593974G>C
GRCh37
NC_000017.9:g.29618087G>C
NCBI36
Search 100 bp 5'
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