Allele Registry

Canonical Allele Identifier: CA12176361

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.417727A>C

GRCh37 chr6:g.417727A>C

Linked Data - Sequence & Population

gnomAD v2:

6:417727 A / C

gnomAD v3:

6:417727 A / C

gnomAD v4:

chr6-417727-A-C

Joint Max Group AF 0.47833584 (NFE)

Genomes Max Group AF 0.47833584 (NFE)

Linked Data - NCBI & NCI

dbSNP:

9378805

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.417727A>C , CM000668.2:g.417727A>C	GRCh38
NC_000006.11:g.417727A>C , CM000668.1:g.417727A>C	GRCh37
NC_000006.10:g.362727A>C	NCBI36

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