Canonical Allele Identifier: CA448985023
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233368T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233140T>C , CM000668.2:g.26233140T>C GRCh38
NC_000006.11:g.26233368T>C , CM000668.1:g.26233368T>C GRCh37
NC_000006.10:g.26341347T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.19T>C