ClinGen Allele Registry
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Canonical Allele Identifier:
CA14932957
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.49957323G>A
GRCh37
chr22:g.50350971G>A
Linked Data - Sequence & Population
gnomAD v2:
22:50350971 G / A
gnomAD v3:
22:49957323 G / A
gnomAD v4:
chr22-49957323-G-A
Joint Max Group AF
0.13398205 (EAS)
Genomes Max Group AF
0.13398205 (EAS)
Linked Data - NCBI & NCI
dbSNP:
28372448
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.49957323G>A , CM000684.2:g.49957323G>A
GRCh38
NC_000022.10:g.50350971G>A , CM000684.1:g.50350971G>A
GRCh37
NC_000022.9:g.48736975G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'