Allele Registry

Canonical Allele Identifier: CA710693597

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr15:g.101267710T>A

GRCh37 chr15:g.101807915T>A

Linked Data - Sequence & Population

gnomAD v3:

15:101267710 T / A

gnomAD v4:

chr15-101267710-T-A

Linked Data - NCBI & NCI

dbSNP:

2101171

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101267710T>A , CM000677.2:g.101267710T>A	GRCh38
NC_000015.9:g.101807915T>A , CM000677.1:g.101807915T>A	GRCh37
NC_000015.8:g.99625438T>A	NCBI36

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