Allele Registry

Canonical Allele Identifier: CA566393327

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.32693166A>T

GRCh37 chr6:g.32660943A>T

Linked Data - Sequence & Population

gnomAD v2:

6:32660943 A / T

gnomAD v3:

6:32693166 A / T

gnomAD v4:

chr6-32693166-A-T

Linked Data - NCBI & NCI

dbSNP:

9275245

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32693166A>T , CM000668.2:g.32693166A>T	GRCh38
NC_000006.11:g.32660943A>T , CM000668.1:g.32660943A>T	GRCh37
NC_000006.10:g.32768921A>T	NCBI36

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