Allele Registry

Canonical Allele Identifier: CA36432682

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.204814890A>C

GRCh37 chr1:g.204784018A>C

Linked Data - Sequence & Population

gnomAD v2:

1:204784018 A / C

gnomAD v3:

1:204814890 A / C

gnomAD v4:

chr1-204814890-A-C

Joint Max Group AF 0.22261798 (AFR)

Genomes Max Group AF 0.22261798 (AFR)

Linked Data - NCBI & NCI

dbSNP:

7552806

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204814890A>C , CM000663.2:g.204814890A>C	GRCh38
NC_000001.10:g.204784018A>C , CM000663.1:g.204784018A>C	GRCh37
NC_000001.9:g.203050641A>C	NCBI36

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