Canonical Allele Identifier: CA448984962

Gene: H2AC9P

Linked Data

• gnomAD v4: 6-26233130-A-G
• MyVariant Identifiers: chr6:g.26233358A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233130A>G , CM000668.2:g.26233130A>G	GRCh38
NC_000006.11:g.26233358A>G , CM000668.1:g.26233358A>G	GRCh37
NC_000006.10:g.26341337A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.9A>G