ClinGen Allele Registry
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Canonical Allele Identifier:
CA16138415
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.27747289C>T
GRCh37
chr3:g.27788780C>T
Linked Data - Sequence & Population
gnomAD v2:
3:27788780 C / T
gnomAD v3:
3:27747289 C / T
gnomAD v4:
chr3-27747289-C-T
Joint Max Group AF
0.74757988 (EAS)
Genomes Max Group AF
0.74757988 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11129295
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.27747289C>T , CM000665.2:g.27747289C>T
GRCh38
NC_000003.11:g.27788780C>T , CM000665.1:g.27788780C>T
GRCh37
NC_000003.10:g.27763784C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'