ClinGen Allele Registry
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Canonical Allele Identifier:
CA15849663
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.78622392C>T
GRCh37
chr15:g.78914734C>T
Linked Data - Sequence & Population
gnomAD v2:
15:78914734 C / T
gnomAD v3:
15:78622392 C / T
gnomAD v4:
chr15-78622392-C-T
Joint Max Group AF
0.80775167 (AFR)
Genomes Max Group AF
0.80775167 (AFR)
Linked Data - NCBI & NCI
dbSNP:
8023462
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.78622392C>T , CM000677.2:g.78622392C>T
GRCh38
NC_000015.9:g.78914734C>T , CM000677.1:g.78914734C>T
GRCh37
NC_000015.8:g.76701789C>T
NCBI36
NG_016143.1:g.3904G>A
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