ClinGen Allele Registry
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Canonical Allele Identifier:
CA14822553
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.55184590G>A
GRCh37
chr20:g.53801129G>A
Linked Data - Sequence & Population
gnomAD v2:
20:53801129 G / A
gnomAD v3:
20:55184590 G / A
gnomAD v4:
chr20-55184590-G-A
Joint Max Group AF
0.35170529 (AFR)
Genomes Max Group AF
0.35170529 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6092078
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.55184590G>A , CM000682.2:g.55184590G>A
GRCh38
NC_000020.10:g.53801129G>A , CM000682.1:g.53801129G>A
GRCh37
NC_000020.9:g.53234536G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'