Canonical Allele Identifier: CA1616962352
Gene: H2AC9P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233187G= , CM000668.2:g.26233187G= GRCh38
NC_000006.11:g.26233415G= , CM000668.1:g.26233415G= GRCh37
NC_000006.10:g.26341394G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.66G=