Allele Registry

Canonical Allele Identifier: CA585790524

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.6365615T>A

GRCh37 chr9:g.6365615T>A

Linked Data - Sequence & Population

gnomAD v2:

9:6365615 T / A

gnomAD v3:

9:6365615 T / A

gnomAD v4:

chr9-6365615-T-A

Linked Data - NCBI & NCI

dbSNP:

1255827185

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6365615T>A , CM000671.2:g.6365615T>A	GRCh38
NC_000009.11:g.6365615T>A , CM000671.1:g.6365615T>A	GRCh37
NC_000009.10:g.6355615T>A	NCBI36

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