Canonical Allele Identifier: CA136260663

Gene: H2AC9P

Linked Data

• dbSNP Id: rs978169093
• gnomAD v2: 6-26233363-A-T
• gnomAD v3: 6-26233135-A-T
• gnomAD v4: 6-26233135-A-T
• MyVariant Identifiers: chr6:g.26233363A>T (hg19) ; chr6:g.26233135A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233135A>T , CM000668.2:g.26233135A>T	GRCh38
NC_000006.11:g.26233363A>T , CM000668.1:g.26233363A>T	GRCh37
NC_000006.10:g.26341342A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.14A>T