ClinGen Allele Registry
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Canonical Allele Identifier:
CA14369282
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.4710335C>T
GRCh37
chr17:g.4613630C>T
Linked Data - Sequence & Population
gnomAD v2:
17:4613630 C / T
gnomAD v3:
17:4710335 C / T
gnomAD v4:
chr17-4710335-C-T
Joint Max Group AF
0.23570416 (NFE)
Genomes Max Group AF
0.23570416 (NFE)
Linked Data - NCBI & NCI
dbSNP:
34230287
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.4710335C>T , CM000679.2:g.4710335C>T
GRCh38
NC_000017.10:g.4613630C>T , CM000679.1:g.4613630C>T
GRCh37
NC_000017.9:g.4560379C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'