Canonical Allele Identifier: CA448985097

Gene: H2AC9P

Linked Data

• dbSNP Id: rs966378887
• MyVariant Identifiers: chr6:g.26233380C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233152C>G , CM000668.2:g.26233152C>G	GRCh38
NC_000006.11:g.26233380C>G , CM000668.1:g.26233380C>G	GRCh37
NC_000006.10:g.26341359C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.31C>G