Allele Registry

Canonical Allele Identifier: CA14406677

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr17:g.55680426T>C

GRCh37 chr17:g.53757787T>C

Linked Data - Sequence & Population

gnomAD v2:

17:53757787 T / C

gnomAD v3:

17:55680426 T / C

gnomAD v4:

chr17-55680426-T-C

Joint Max Group AF 0.80620137 (AFR)

Genomes Max Group AF 0.80620137 (AFR)

Linked Data - NCBI & NCI

dbSNP:

1549519

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.55680426T>C , CM000679.2:g.55680426T>C	GRCh38
NC_000017.10:g.53757787T>C , CM000679.1:g.53757787T>C	GRCh37
NC_000017.9:g.51112786T>C	NCBI36

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