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Canonical Allele Identifier:
CA16546587
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.78212770C>T
GRCh37
chr17:g.76208851C>T
Linked Data - Sequence & Population
gnomAD v2:
17:76208851 C / T
gnomAD v3:
17:78212770 C / T
gnomAD v4:
chr17-78212770-C-T
Joint Max Group AF
0.85547229 (AFR)
Genomes Max Group AF
0.85547229 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3764383
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.78212770C>T , CM000679.2:g.78212770C>T
GRCh38
NC_000017.10:g.76208851C>T , CM000679.1:g.76208851C>T
GRCh37
NC_000017.9:g.73720446C>T
NCBI36
NG_029069.1:g.3575C>T
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