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Canonical Allele Identifier:
CA12685098
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.42345021T>C
GRCh37
chr7:g.42384620T>C
Linked Data - Sequence & Population
gnomAD v2:
7:42384620 T / C
gnomAD v3:
7:42345021 T / C
gnomAD v4:
chr7-42345021-T-C
Joint Max Group AF
0.80389878 (AMR)
Genomes Max Group AF
0.80389878 (AMR)
Linked Data - NCBI & NCI
dbSNP:
7791745
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.42345021T>C , CM000669.2:g.42345021T>C
GRCh38
NC_000007.13:g.42384620T>C , CM000669.1:g.42384620T>C
GRCh37
NC_000007.12:g.42351145T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'