Canonical Allele Identifier: CA448985337
Gene: H2AC9P HGNC NCBI

Linked Data

dbSNP Id: rs909316688
gnomAD v4: 6-26233193-C-A
MyVariant Identifiers: chr6:g.26233421C>A (hg19) chr6:g.26233193C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233193C>A , CM000668.2:g.26233193C>A GRCh38
NC_000006.11:g.26233421C>A , CM000668.1:g.26233421C>A GRCh37
NC_000006.10:g.26341400C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.72C>A
Search 100 bp 5'
Search 100 bp 3'