ClinGen Allele Registry
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Canonical Allele Identifier:
CA14538412
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.59836146G>A
GRCh37
chr18:g.57503378G>A
Linked Data - Sequence & Population
gnomAD v2:
18:57503378 G / A
gnomAD v3:
18:59836146 G / A
gnomAD v4:
chr18-59836146-G-A
Joint Max Group AF
0.3781367 (AFR)
Genomes Max Group AF
0.3781367 (AFR)
Linked Data - NCBI & NCI
dbSNP:
8093763
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.59836146G>A , CM000680.2:g.59836146G>A
GRCh38
NC_000018.9:g.57503378G>A , CM000680.1:g.57503378G>A
GRCh37
NC_000018.8:g.55654358G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'