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Canonical Allele Identifier:
CA14085622
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.70506220C>T
GRCh37
chr15:g.70798559C>T
Linked Data - Sequence & Population
gnomAD v2:
15:70798559 C / T
gnomAD v3:
15:70506220 C / T
gnomAD v4:
chr15-70506220-C-T
Joint Max Group AF
0.63029927 (EAS)
Genomes Max Group AF
0.63029927 (EAS)
Linked Data - NCBI & NCI
dbSNP:
8034004
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.70506220C>T , CM000677.2:g.70506220C>T
GRCh38
NC_000015.9:g.70798559C>T , CM000677.1:g.70798559C>T
GRCh37
NC_000015.8:g.68585613C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'