ClinGen Allele Registry
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Canonical Allele Identifier:
CA281566240
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.50952397G>A
GRCh37
chr16:g.50986308G>A
Linked Data - Sequence & Population
gnomAD v2:
16:50986308 G / A
gnomAD v3:
16:50952397 G / A
gnomAD v4:
chr16-50952397-G-A
Joint Max Group AF
0.85419065 (AFR)
Genomes Max Group AF
0.85419065 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1564981
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.50952397G>A , CM000678.2:g.50952397G>A
GRCh38
NC_000016.9:g.50986308G>A , CM000678.1:g.50986308G>A
GRCh37
NC_000016.8:g.49543809G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'