Canonical Allele Identifier: CA448985089

Gene: H2AC9P

Linked Data

• gnomAD v4: 6-26233151-G-A
• MyVariant Identifiers: chr6:g.26233379G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233151G>A , CM000668.2:g.26233151G>A	GRCh38
NC_000006.11:g.26233379G>A , CM000668.1:g.26233379G>A	GRCh37
NC_000006.10:g.26341358G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.30G>A