Canonical Allele Identifier: CA448985621

Gene: H2AC9P

Linked Data

• dbSNP Id: rs1759684866
• MyVariant Identifiers: chr6:g.26233469C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233241C>G , CM000668.2:g.26233241C>G	GRCh38
NC_000006.11:g.26233469C>G , CM000668.1:g.26233469C>G	GRCh37
NC_000006.10:g.26341448C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.120C>G