Allele Registry

Canonical Allele Identifier: CA102679399

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr4:g.102225733A>T

GRCh38 chr4:g.102225733_102225739delinsTTGCTTT

GRCh37 chr4:g.103146890A>T

GRCh37 chr4:g.103146890_103146896delinsTTGCTTT

Linked Data - Sequence & Population

gnomAD v2:

4:103146890 A / T

gnomAD v3:

4:102225733 A / T

gnomAD v4:

chr4-102225733-A-T

Joint Max Group AF 0.08215979 (NFE)

Genomes Max Group AF 0.08215979 (NFE)

Linked Data - NCBI & NCI

dbSNP:

35518360

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102225733A>T , CM000666.2:g.102225733A>T	GRCh38
NC_000004.11:g.103146890A>T , CM000666.1:g.103146890A>T	GRCh37
NC_000004.10:g.103365913A>T	NCBI36

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