ClinGen Allele Registry
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Canonical Allele Identifier:
CA262598326
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.73136377C>T
GRCh37
chr14:g.73603085C>T
Linked Data - Sequence & Population
gnomAD v3:
14:73136377 C / T
gnomAD v4:
chr14-73136377-C-T
Joint Max Group AF
0.00007271 (SAS)
Genomes Max Group AF
0.00007285 (SAS)
Linked Data - NCBI & NCI
dbSNP:
563558461
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.73136377C>T , CM000676.2:g.73136377C>T
GRCh38
NC_000014.8:g.73603085C>T , CM000676.1:g.73603085C>T
GRCh37
NC_000014.7:g.72672838C>T
NCBI36
NG_007386.2:g.4907C>T
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