Canonical Allele Identifier: CA136260712

Gene: H2AC9P

Linked Data

• dbSNP Id: rs909316688
• gnomAD v3: 6-26233193-C-G
• gnomAD v4: 6-26233193-C-G
• MyVariant Identifiers: chr6:g.26233421C>G (hg19) ; chr6:g.26233193C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233193C>G , CM000668.2:g.26233193C>G	GRCh38
NC_000006.11:g.26233421C>G , CM000668.1:g.26233421C>G	GRCh37
NC_000006.10:g.26341400C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.72C>G