ClinGen Allele Registry
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Canonical Allele Identifier:
CA14707849
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.22176638C>T
GRCh37
chr19:g.22359440C>T
Linked Data - Sequence & Population
gnomAD v2:
19:22359440 C / T
gnomAD v3:
19:22176638 C / T
gnomAD v4:
chr19-22176638-C-T
Joint Max Group AF
0.57017907 (AFR)
Genomes Max Group AF
0.57017907 (AFR)
Linked Data - NCBI & NCI
dbSNP:
412658
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.22176638C>T , CM000681.2:g.22176638C>T
GRCh38
NC_000019.9:g.22359440C>T , CM000681.1:g.22359440C>T
GRCh37
NC_000019.8:g.22151280C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'