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Canonical Allele Identifier:
CA16306849
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.86284446T>C
GRCh37
chr7:g.85913762T>C
Linked Data - Sequence & Population
gnomAD v2:
7:85913762 T / C
gnomAD v3:
7:86284446 T / C
gnomAD v4:
chr7-86284446-T-C
Joint Max Group AF
0.90285063 (SAS)
Genomes Max Group AF
0.90285063 (SAS)
Linked Data - NCBI & NCI
dbSNP:
2708553
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.86284446T>C , CM000669.2:g.86284446T>C
GRCh38
NC_000007.13:g.85913762T>C , CM000669.1:g.85913762T>C
GRCh37
NC_000007.12:g.85751698T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'