ClinGen Allele Registry
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Canonical Allele Identifier:
CA166598471
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.124366686C>T
GRCh37
chr7:g.124006740C>T
Linked Data - Sequence & Population
gnomAD v2:
7:124006740 C / T
gnomAD v3:
7:124366686 C / T
gnomAD v4:
chr7-124366686-C-T
Joint Max Group AF
0.24405873 (EAS)
Genomes Max Group AF
0.24405873 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17147033
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.124366686C>T , CM000669.2:g.124366686C>T
GRCh38
NC_000007.13:g.124006740C>T , CM000669.1:g.124006740C>T
GRCh37
NC_000007.12:g.123793976C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'