Canonical Allele Identifier: CA448985413
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233436T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233208T>A , CM000668.2:g.26233208T>A GRCh38
NC_000006.11:g.26233436T>A , CM000668.1:g.26233436T>A GRCh37
NC_000006.10:g.26341415T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.87T>A
Search 100 bp 5'
Search 100 bp 3'