Canonical Allele Identifier: CA448985199
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233398T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233170T>A , CM000668.2:g.26233170T>A GRCh38
NC_000006.11:g.26233398T>A , CM000668.1:g.26233398T>A GRCh37
NC_000006.10:g.26341377T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.49T>A