Canonical Allele Identifier: CA448985410

Gene: H2AC9P

Linked Data

• dbSNP Id: rs1581469254
• MyVariant Identifiers: chr6:g.26233435C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233207C>T , CM000668.2:g.26233207C>T	GRCh38
NC_000006.11:g.26233435C>T , CM000668.1:g.26233435C>T	GRCh37
NC_000006.10:g.26341414C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.86C>T