Canonical Allele Identifier: CA448985152
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233389A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233161A>T , CM000668.2:g.26233161A>T GRCh38
NC_000006.11:g.26233389A>T , CM000668.1:g.26233389A>T GRCh37
NC_000006.10:g.26341368A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.40A>T