Allele Registry

Canonical Allele Identifier: CA15597230

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr9:g.16368734G>T

GRCh37 chr9:g.16368732G>T

Linked Data - Sequence & Population

gnomAD v2:

9:16368732 G / T

gnomAD v3:

9:16368734 G / T

gnomAD v4:

chr9-16368734-G-T

Joint Max Group AF 0.448128 (SAS)

Genomes Max Group AF 0.448128 (SAS)

Linked Data - NCBI & NCI

dbSNP:

7864648

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.16368734G>T , CM000671.2:g.16368734G>T	GRCh38
NC_000009.11:g.16368732G>T , CM000671.1:g.16368732G>T	GRCh37
NC_000009.10:g.16358732G>T	NCBI36

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