ClinGen Allele Registry
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Canonical Allele Identifier:
CA14933339
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr22:g.50666252G>A
GRCh37
chr22:g.51104680G>A
Linked Data - Sequence & Population
gnomAD v2:
22:51104680 G / A
gnomAD v3:
22:50666252 G / A
gnomAD v4:
chr22-50666252-G-A
Joint Max Group AF
0.44438003 (NFE)
Genomes Max Group AF
0.44438003 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9616906
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.50666252G>A , CM000684.2:g.50666252G>A
GRCh38
NC_000022.10:g.51104680G>A , CM000684.1:g.51104680G>A
GRCh37
NC_000022.9:g.49451546G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'