Canonical Allele Identifier: CA12350522

Gene: H2AC9P

Linked Data

• dbSNP Id: rs183498674
• gnomAD v2: 6-26233406-A-G
• gnomAD v3: 6-26233178-A-G
• gnomAD v4: 6-26233178-A-G
• MyVariant Identifiers: chr6:g.26233406A>G (hg19) ; chr6:g.26233178A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233178A>G , CM000668.2:g.26233178A>G	GRCh38
NC_000006.11:g.26233406A>G , CM000668.1:g.26233406A>G	GRCh37
NC_000006.10:g.26341385A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.57A>G