Allele Registry

Canonical Allele Identifier: CA168563310

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr7:g.146115955T>G

GRCh37 chr7:g.145813047T>G

Linked Data - Sequence & Population

gnomAD v2:

7:145813047 T / G

gnomAD v3:

7:146115955 T / G

gnomAD v4:

chr7-146115955-T-G

Joint Max Group AF 0.02339205 (MID)

Genomes Max Group AF 0.01750981 (NFE)

Exomes Max Group AF 0.02132281 (NFE)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001433595

ClinVar Variation:

1108205

dbSNP:

150447075

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.146115955T>G , CM000669.2:g.146115955T>G	GRCh38
NC_000007.13:g.145813047T>G , CM000669.1:g.145813047T>G	GRCh37
NC_000007.12:g.145443980T>G	NCBI36
NG_007092.2:g.4595T>G
NG_007092.3:g.4955T>G

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