ClinGen Allele Registry
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Canonical Allele Identifier:
CA14617333
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.60246201G>A
GRCh37
chr18:g.57913434G>A
Linked Data - Sequence & Population
gnomAD v2:
18:57913434 G / A
gnomAD v3:
18:60246201 G / A
gnomAD v4:
chr18-60246201-G-A
Joint Max Group AF
0.42144455 (SAS)
Genomes Max Group AF
0.42144455 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4450508
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.60246201G>A , CM000680.2:g.60246201G>A
GRCh38
NC_000018.9:g.57913434G>A , CM000680.1:g.57913434G>A
GRCh37
NC_000018.8:g.56064414G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'