Canonical Allele Identifier: CA357516978

Gene: H2AZ1

Linked Data

• gnomAD v4: 4-99949701-T-A
• MyVariant Identifiers: chr4:g.100870858T>A (hg19) ; chr4:g.99949701T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99949701T>A , CM000666.2:g.99949701T>A	GRCh38
NC_000004.11:g.100870858T>A , CM000666.1:g.100870858T>A	GRCh37
NC_000004.10:g.101089881T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296417.6:c.43A>T MANE Select	ENSP00000296417.5:p.Thr15Ser
ENST00000651623.1:c.43A>T	ENSP00000498935.1:p.Thr15Ser
ENST00000296417.5:c.43A>T	ENSP00000296417.5:p.Thr15Ser
ENST00000511203.1:n.599A>T
ENST00000511319.5:n.568A>T
ENST00000511348.1:n.228A>T
ENST00000527366.1:n.127A>T
ENST00000529158.5:n.92A>T
NM_002106.3:c.43A>T	NP_002097.1:p.Thr15Ser
NM_002106.4:c.43A>T MANE Select	NP_002097.1:p.Thr15Ser