Canonical Allele Identifier: CA553568694

Gene: H2AZ1

Linked Data

• dbSNP Id: rs1435575753
• gnomAD v2: 4-100870661-A-ACGTGATTC
• MyVariant Identifiers: chr4:g.100870661_100870662insCGTGATTC (hg19) ; chr4:g.99949504_99949505insCGTGATTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949506_99949513dup , CM000666.2:g.99949506_99949513dup	GRCh38
NC_000004.11:g.100870663_100870670dup , CM000666.1:g.100870663_100870670dup	GRCh37
NC_000004.10:g.101089686_101089693dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.82-126_82-119dup MANE Select	ENSP00000296417.5:n.82-126_82-119dup
ENST00000651623.1:c.82-126_82-119dup	ENSP00000498935.1:n.82-126_82-119dup
ENST00000296417.5:c.82-126_82-119dup	ENSP00000296417.5:n.82-126_82-119dup
ENST00000511203.1:n.788_795dup
ENST00000511319.5:n.607-126_607-119dup
ENST00000511348.1:n.417_424dup
ENST00000527366.1:n.166-133_166-126dup
ENST00000529158.5:n.131-126_131-119dup
NM_002106.3:c.82-126_82-119dup	NP_002097.1:n.82-126_82-119dup
NM_002106.4:c.82-126_82-119dup MANE Select	NP_002097.1:n.82-126_82-119dup