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Canonical Allele Identifier:
CA183922019
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.112061867C>T
GRCh37
chr8:g.113074096C>T
Linked Data - Sequence & Population
gnomAD v2:
8:113074096 C / T
gnomAD v3:
8:112061867 C / T
gnomAD v4:
chr8-112061867-C-T
Joint Max Group AF
0.70318451 (AFR)
Genomes Max Group AF
0.70318451 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1996720
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.112061867C>T , CM000670.2:g.112061867C>T
GRCh38
NC_000008.10:g.113074096C>T , CM000670.1:g.113074096C>T
GRCh37
NC_000008.9:g.113143272C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'