Canonical Allele Identifier: CA1616962342
Gene: H2AC9P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233165G= , CM000668.2:g.26233165G= GRCh38
NC_000006.11:g.26233393G= , CM000668.1:g.26233393G= GRCh37
NC_000006.10:g.26341372G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.44G=