Canonical Allele Identifier: CA448985019
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233367C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233139C>T , CM000668.2:g.26233139C>T GRCh38
NC_000006.11:g.26233367C>T , CM000668.1:g.26233367C>T GRCh37
NC_000006.10:g.26341346C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.18C>T