ClinGen Allele Registry
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Canonical Allele Identifier:
CA863496530
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.34710263G>C
GRCh37
chr9:g.34710260G>C
Linked Data - Sequence & Population
gnomAD v4:
chr9-34710263-G-C
Joint Max Group AF
0.000001 (NFE)
Exomes Max Group AF
0.00000126 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2812378
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.34710263G>C , CM000671.2:g.34710263G>C
GRCh38
NC_000009.11:g.34710260G>C , CM000671.1:g.34710260G>C
GRCh37
NC_000009.10:g.34700260G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'