Allele Registry

Canonical Allele Identifier: CA11919446

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr5:g.6834054T>C

GRCh37 chr5:g.6834167T>C

Linked Data - Sequence & Population

gnomAD v2:

5:6834167 T / C

gnomAD v3:

5:6834054 T / C

gnomAD v4:

chr5-6834054-T-C

Joint Max Group AF 0.05509583 (NFE)

Genomes Max Group AF 0.05509583 (NFE)

Linked Data - NCBI & NCI

dbSNP:

11134178

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6834054T>C , CM000667.2:g.6834054T>C	GRCh38
NC_000005.9:g.6834167T>C , CM000667.1:g.6834167T>C	GRCh37
NC_000005.8:g.6887167T>C	NCBI36

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