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Canonical Allele Identifier:
CA11933639
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.76714881C>T
GRCh37
chr5:g.76010706C>T
Linked Data - Sequence & Population
gnomAD v2:
5:76010706 C / T
gnomAD v3:
5:76714881 C / T
gnomAD v4:
chr5-76714881-C-T
Joint Max Group AF
0.3931268 (EAS)
Genomes Max Group AF
0.3931268 (EAS)
Linked Data - NCBI & NCI
dbSNP:
32934
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.76714881C>T , CM000667.2:g.76714881C>T
GRCh38
NC_000005.9:g.76010706C>T , CM000667.1:g.76010706C>T
GRCh37
NC_000005.8:g.76046462C>T
NCBI36
NG_032906.1:g.3839C>T
Search 100 bp 5'
Search 100 bp 3'