Canonical Allele Identifier: CA448985186
Gene: H2AC9P HGNC NCBI

Linked Data

gnomAD v4: 6-26233167-C-T
MyVariant Identifiers: chr6:g.26233395C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233167C>T , CM000668.2:g.26233167C>T GRCh38
NC_000006.11:g.26233395C>T , CM000668.1:g.26233395C>T GRCh37
NC_000006.10:g.26341374C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.46C>T