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Canonical Allele Identifier:
CA15616405
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.105664781C>T
GRCh37
chr9:g.108427062C>T
Linked Data - Sequence & Population
gnomAD v2:
9:108427062 C / T
gnomAD v3:
9:105664781 C / T
gnomAD v4:
chr9-105664781-C-T
Joint Max Group AF
0.47159801 (EAS)
Genomes Max Group AF
0.47159801 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1463984
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.105664781C>T , CM000671.2:g.105664781C>T
GRCh38
NC_000009.11:g.108427062C>T , CM000671.1:g.108427062C>T
GRCh37
NC_000009.10:g.107466883C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'