Canonical Allele Identifier: CA448985379

Gene: H2AC9P

Linked Data

• gnomAD v4: 6-26233201-C-T
• MyVariant Identifiers: chr6:g.26233429C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233201C>T , CM000668.2:g.26233201C>T	GRCh38
NC_000006.11:g.26233429C>T , CM000668.1:g.26233429C>T	GRCh37
NC_000006.10:g.26341408C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.80C>T