Canonical Allele Identifier: CA448986247
Gene: H2AC9P HGNC NCBI

Linked Data

gnomAD v4: 6-26233252-G-T
MyVariant Identifiers: chr6:g.26233480G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233252G>T , CM000668.2:g.26233252G>T GRCh38
NC_000006.11:g.26233480G>T , CM000668.1:g.26233480G>T GRCh37
NC_000006.10:g.26341459G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.131G>T
Search 100 bp 5'
Search 100 bp 3'