ClinGen Allele Registry
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Canonical Allele Identifier:
CA12569485
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.100914499C>T
GRCh37
chr7:g.100512119C>T
Linked Data - Sequence & Population
gnomAD v2:
7:100512119 C / T
gnomAD v3:
7:100914499 C / T
gnomAD v4:
chr7-100914499-C-T
Joint Max Group AF
0.80573273 (EAS)
Genomes Max Group AF
0.80573273 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6976053
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.100914499C>T , CM000669.2:g.100914499C>T
GRCh38
NC_000007.13:g.100512119C>T , CM000669.1:g.100512119C>T
GRCh37
NC_000007.12:g.100350055C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'