ClinGen Allele Registry
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Canonical Allele Identifier:
CA14944243
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.46025962G>T
GRCh37
chr22:g.46421842G>T
Linked Data - Sequence & Population
gnomAD v2:
22:46421842 G / T
gnomAD v3:
22:46025962 G / T
gnomAD v4:
chr22-46025962-G-T
Joint Max Group AF
0.81983205 (AFR)
Genomes Max Group AF
0.81983205 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6519955
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.46025962G>T , CM000684.2:g.46025962G>T
GRCh38
NC_000022.10:g.46421842G>T , CM000684.1:g.46421842G>T
GRCh37
NC_000022.9:g.44800506G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'