Canonical Allele Identifier: CA448985559
Gene: H2AC9P HGNC NCBI

Linked Data

dbSNP Id: rs1291904566
gnomAD v3: 6-26233232-T-G
gnomAD v4: 6-26233232-T-G
MyVariant Identifiers: chr6:g.26233460T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233232T>G , CM000668.2:g.26233232T>G GRCh38
NC_000006.11:g.26233460T>G , CM000668.1:g.26233460T>G GRCh37
NC_000006.10:g.26341439T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000403259.1:n.111T>G