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Canonical Allele Identifier:
CA16222166
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.25898812T>C
GRCh37
chr5:g.25898921T>C
Linked Data - Sequence & Population
gnomAD v2:
5:25898921 T / C
gnomAD v3:
5:25898812 T / C
gnomAD v4:
chr5-25898812-T-C
Joint Max Group AF
0.37545692 (NFE)
Genomes Max Group AF
0.37545692 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7704909
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.25898812T>C , CM000667.2:g.25898812T>C
GRCh38
NC_000005.9:g.25898921T>C , CM000667.1:g.25898921T>C
GRCh37
NC_000005.8:g.25934678T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'