ClinGen Allele Registry
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Canonical Allele Identifier:
CA14447298
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.30295210A>G
GRCh37
chr17:g.28622228A>G
Linked Data - Sequence & Population
gnomAD v2:
17:28622228 A / G
gnomAD v3:
17:30295210 A / G
gnomAD v4:
chr17-30295210-A-G
Joint Max Group AF
0.8744208 (AFR)
Genomes Max Group AF
0.8744208 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11867581
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.30295210A>G , CM000679.2:g.30295210A>G
GRCh38
NC_000017.10:g.28622228A>G , CM000679.1:g.28622228A>G
GRCh37
NC_000017.9:g.25646354A>G
NCBI36
NG_011440.1:g.1847T>C
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