Canonical Allele Identifier: CA448985427
Gene: H2AC9P HGNC NCBI

Linked Data

dbSNP Id: rs1210077851
gnomAD v4: 6-26233211-G-A
MyVariant Identifiers: chr6:g.26233439G>A (hg19) chr6:g.26233211G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233211G>A , CM000668.2:g.26233211G>A GRCh38
NC_000006.11:g.26233439G>A , CM000668.1:g.26233439G>A GRCh37
NC_000006.10:g.26341418G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.90G>A
Search 100 bp 5'
Search 100 bp 3'