Canonical Allele Identifier: CA448984966

Gene: H2AC9P

Linked Data

• dbSNP Id: rs1444713683
• gnomAD v3: 6-26233131-A-C
• gnomAD v4: 6-26233131-A-C
• MyVariant Identifiers: chr6:g.26233359A>C (hg19) ; chr6:g.26233131A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233131A>C , CM000668.2:g.26233131A>C	GRCh38
NC_000006.11:g.26233359A>C , CM000668.1:g.26233359A>C	GRCh37
NC_000006.10:g.26341338A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.10A>C