Canonical Allele Identifier: CA448985049
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233372T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233144T>G , CM000668.2:g.26233144T>G GRCh38
NC_000006.11:g.26233372T>G , CM000668.1:g.26233372T>G GRCh37
NC_000006.10:g.26341351T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.23T>G