Canonical Allele Identifier: CA448985160
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233391T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233163T>C , CM000668.2:g.26233163T>C GRCh38
NC_000006.11:g.26233391T>C , CM000668.1:g.26233391T>C GRCh37
NC_000006.10:g.26341370T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.42T>C