ClinGen Allele Registry
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Canonical Allele Identifier:
CA14640571
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.32873722C>T
GRCh37
chr19:g.33364628C>T
Linked Data - Sequence & Population
gnomAD v2:
19:33364628 C / T
gnomAD v3:
19:32873722 C / T
gnomAD v4:
chr19-32873722-C-T
Joint Max Group AF
0.60253231 (NFE)
Genomes Max Group AF
0.60253231 (NFE)
Linked Data - NCBI & NCI
dbSNP:
8101881
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.32873722C>T , CM000681.2:g.32873722C>T
GRCh38
NC_000019.9:g.33364628C>T , CM000681.1:g.33364628C>T
GRCh37
NC_000019.8:g.38056468C>T
NCBI36
NG_008258.1:g.1056G>A
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