Allele Registry

Canonical Allele Identifier: CA12184963

Gene: H2AC9P HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr6:g.26233159A>G

GRCh37 chr6:g.26233387A>G

Linked Data - Sequence & Population

gnomAD v2:

6:26233387 A / G

gnomAD v3:

6:26233159 A / G

gnomAD v4:

chr6-26233159-A-G

Joint Max Group AF 0.74356754 (EAS)

Genomes Max Group AF 0.74356754 (EAS)

Linked Data - NCBI & NCI

dbSNP:

10946808

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233159A>G , CM000668.2:g.26233159A>G	GRCh38
NC_000006.11:g.26233387A>G , CM000668.1:g.26233387A>G	GRCh37
NC_000006.10:g.26341366A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.38A>G

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