Allele Registry

Canonical Allele Identifier: CA114214586

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.9623994C>A

GRCh37 chr5:g.9624106C>A

Linked Data - Sequence & Population

gnomAD v2:

5:9624106 C / A

gnomAD v3:

5:9623994 C / A

gnomAD v4:

chr5-9623994-C-A

Joint Max Group AF 0.05949011 (AFR)

Genomes Max Group AF 0.05949011 (AFR)

Linked Data - NCBI & NCI

dbSNP:

10513026

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.9623994C>A , CM000667.2:g.9623994C>A	GRCh38
NC_000005.9:g.9624106C>A , CM000667.1:g.9624106C>A	GRCh37
NC_000005.8:g.9677106C>A	NCBI36

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