Canonical Allele Identifier: CA448985390

Gene: H2AC9P

Linked Data

• gnomAD v4: 6-26233204-C-T
• MyVariant Identifiers: chr6:g.26233432C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233204C>T , CM000668.2:g.26233204C>T	GRCh38
NC_000006.11:g.26233432C>T , CM000668.1:g.26233432C>T	GRCh37
NC_000006.10:g.26341411C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.83C>T