Canonical Allele Identifier: CA136260718

Gene: H2AC9P

Linked Data

• dbSNP Id: rs907200472
• gnomAD v3: 6-26233214-C-T
• gnomAD v4: 6-26233214-C-T
• MyVariant Identifiers: chr6:g.26233442C>T (hg19) ; chr6:g.26233214C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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