Canonical Allele Identifier: CA448985061

Gene: H2AC9P

Linked Data

• gnomAD v4: 6-26233146-G-T
• MyVariant Identifiers: chr6:g.26233374G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233146G>T , CM000668.2:g.26233146G>T	GRCh38
NC_000006.11:g.26233374G>T , CM000668.1:g.26233374G>T	GRCh37
NC_000006.10:g.26341353G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.25G>T