ClinGen Allele Registry
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Canonical Allele Identifier:
CA14024694
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.101008533C>T
GRCh37
chr14:g.101474870C>T
Linked Data - Sequence & Population
gnomAD v2:
14:101474870 C / T
gnomAD v3:
14:101008533 C / T
gnomAD v4:
chr14-101008533-C-T
Joint Max Group AF
0.2094788 (AFR)
Genomes Max Group AF
0.2094788 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10145110
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.101008533C>T , CM000676.2:g.101008533C>T
GRCh38
NC_000014.8:g.101474870C>T , CM000676.1:g.101474870C>T
GRCh37
NC_000014.7:g.100544623C>T
NCBI36
NG_045000.5:g.177265C>T
NG_045000.6:g.177265C>T
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