Allele Registry

Canonical Allele Identifier: CA880172527

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrX:g.98609356T>A

GRCh37 chrX:g.97864354T>A

Linked Data - Sequence & Population

gnomAD v3:

X:98609356 T / A

gnomAD v4:

chrX-98609356-T-A

Linked Data - NCBI & NCI

dbSNP:

4827947

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.98609356T>A , CM000685.2:g.98609356T>A	GRCh38
NC_000023.10:g.97864354T>A , CM000685.1:g.97864354T>A	GRCh37
NC_000023.9:g.97751010T>A	NCBI36

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