Allele Registry

Canonical Allele Identifier: CA266791712

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr14:g.106704673G>C

Linked Data - Sequence & Population

gnomAD v3:

14:106704673 G / C

gnomAD v4:

chr14-106704673-G-C

Joint Max Group AF 0.15517307 (AFR)

Genomes Max Group AF 0.15517307 (AFR)

Linked Data - NCBI & NCI

dbSNP:

7145100

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.106704673G>C , CM000676.2:g.106704673G>C	GRCh38

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