Canonical Allele Identifier: CA448985002

Gene: H2AC9P

Linked Data

• gnomAD v4: 6-26233137-A-C
• MyVariant Identifiers: chr6:g.26233365A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233137A>C , CM000668.2:g.26233137A>C	GRCh38
NC_000006.11:g.26233365A>C , CM000668.1:g.26233365A>C	GRCh37
NC_000006.10:g.26341344A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.16A>C