ClinGen Allele Registry
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Canonical Allele Identifier:
CA14369290
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr17:g.4721864G>A
GRCh37
chr17:g.4625159G>A
Linked Data - Sequence & Population
gnomAD v2:
17:4625159 G / A
gnomAD v3:
17:4721864 G / A
gnomAD v4:
chr17-4721864-G-A
Joint Max Group AF
0.80125306 (EAS)
Genomes Max Group AF
0.80125306 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2036657
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.4721864G>A , CM000679.2:g.4721864G>A
GRCh38
NC_000017.10:g.4625159G>A , CM000679.1:g.4625159G>A
GRCh37
NC_000017.9:g.4571908G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'