Canonical Allele Identifier: CA1616962344
Gene: H2AC9P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233170T= , CM000668.2:g.26233170T= GRCh38
NC_000006.11:g.26233398T= , CM000668.1:g.26233398T= GRCh37
NC_000006.10:g.26341377T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.49T=