Canonical Allele Identifier: CA136260723

Gene: H2AC9P

Linked Data

• dbSNP Id: rs966114285
• gnomAD v2: 6-26233449-G-A
• gnomAD v3: 6-26233221-G-A
• gnomAD v4: 6-26233221-G-A
• MyVariant Identifiers: chr6:g.26233449G>A (hg19) ; chr6:g.26233221G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26233221G>A , CM000668.2:g.26233221G>A	GRCh38
NC_000006.11:g.26233449G>A , CM000668.1:g.26233449G>A	GRCh37
NC_000006.10:g.26341428G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403259.1:n.100G>A