Canonical Allele Identifier: CA448985070
Gene: H2AC9P HGNC NCBI

Linked Data

gnomAD v4: 6-26233148-C-A
MyVariant Identifiers: chr6:g.26233376C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233148C>A , CM000668.2:g.26233148C>A GRCh38
NC_000006.11:g.26233376C>A , CM000668.1:g.26233376C>A GRCh37
NC_000006.10:g.26341355C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.27C>A