Canonical Allele Identifier: CA448985031
Gene: H2AC9P HGNC NCBI

Linked Data

gnomAD v4: 6-26233141-G-T
MyVariant Identifiers: chr6:g.26233369G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233141G>T , CM000668.2:g.26233141G>T GRCh38
NC_000006.11:g.26233369G>T , CM000668.1:g.26233369G>T GRCh37
NC_000006.10:g.26341348G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.20G>T
Search 100 bp 5'
Search 100 bp 3'