Allele Registry

Canonical Allele Identifier: CA304901017

Gene:

Linked Data

ClinVar RCV:

RCV000005739

RCV000005740

RCV000005741

ClinVar Variation:

5408

dbSNP:

4804803

gnomAD v2:

19:7812733 A / G

gnomAD v3:

19:7747847 A / G

gnomAD v4:

chr19-7747847-A-G

Joint Max Group AF 0.40699696 (AFR)

Genomes Max Group AF 0.40699696 (AFR)

MyVariant.info:

GRCh38 chr19:g.7747847A>G

GRCh37 chr19:g.7812733A>G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7747847A>G , CM000681.2:g.7747847A>G	GRCh38
NC_000019.9:g.7812733A>G , CM000681.1:g.7812733A>G	GRCh37
NC_000019.8:g.7718733A>G	NCBI36
NG_012167.1:g.4732T>C

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