Canonical Allele Identifier: CA1616962345
Gene: H2AC9P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233172G= , CM000668.2:g.26233172G= GRCh38
NC_000006.11:g.26233400G= , CM000668.1:g.26233400G= GRCh37
NC_000006.10:g.26341379G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.51G=