Canonical Allele Identifier: CA448985519

Gene: H2AC9P

Linked Data

• gnomAD v4: 6-26233227-C-A
• MyVariant Identifiers: chr6:g.26233455C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233227C>A , CM000668.2:g.26233227C>A	GRCh38
NC_000006.11:g.26233455C>A , CM000668.1:g.26233455C>A	GRCh37
NC_000006.10:g.26341434C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.106C>A