ClinGen Allele Registry
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Canonical Allele Identifier:
CA14378566
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.40618898C>T
GRCh37
chr17:g.38775150C>T
Linked Data - Sequence & Population
gnomAD v2:
17:38775150 C / T
gnomAD v3:
17:40618898 C / T
gnomAD v4:
chr17-40618898-C-T
Joint Max Group AF
0.794437 (AFR)
Genomes Max Group AF
0.794437 (AFR)
Linked Data - NCBI & NCI
dbSNP:
757411
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.40618898C>T , CM000679.2:g.40618898C>T
GRCh38
NC_000017.10:g.38775150C>T , CM000679.1:g.38775150C>T
GRCh37
NC_000017.9:g.36028676C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'