Canonical Allele Identifier: CA448985439

Gene: H2AC9P

Linked Data

• dbSNP Id: rs907200472
• MyVariant Identifiers: chr6:g.26233442C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233214C>A , CM000668.2:g.26233214C>A	GRCh38
NC_000006.11:g.26233442C>A , CM000668.1:g.26233442C>A	GRCh37
NC_000006.10:g.26341421C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.93C>A