ClinGen Allele Registry
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Canonical Allele Identifier:
CA288533341
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.13159478G>A
GRCh37
chr17:g.13062795G>A
Linked Data - Sequence & Population
gnomAD v2:
17:13062795 G / A
gnomAD v3:
17:13159478 G / A
gnomAD v4:
chr17-13159478-G-A
Joint Max Group AF
0.09967702 (AFR)
Genomes Max Group AF
0.09967702 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9900808
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.13159478G>A , CM000679.2:g.13159478G>A
GRCh38
NC_000017.10:g.13062795G>A , CM000679.1:g.13062795G>A
GRCh37
NC_000017.9:g.13003520G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'