Canonical Allele Identifier: CA1616962380
Gene: H2AC9P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233242T= , CM000668.2:g.26233242T= GRCh38
NC_000006.11:g.26233470T= , CM000668.1:g.26233470T= GRCh37
NC_000006.10:g.26341449T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.121T=