Canonical Allele Identifier: CA1480239152
Gene: H2AZ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949723T= , CM000666.2:g.99949723T= GRCh38
NC_000004.11:g.100870880T= , CM000666.1:g.100870880T= GRCh37
NC_000004.10:g.101089903T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.21A= MANE Select ENSP00000296417.5:p.Gly7=
ENST00000651623.1:c.21A= ENSP00000498935.1:p.Gly7=
ENST00000296417.5:c.21A= ENSP00000296417.5:p.Gly7=
ENST00000511203.1:n.577A=
ENST00000511319.5:n.546A=
ENST00000511348.1:n.206A=
ENST00000527366.1:n.105A=
ENST00000529158.5:n.70A=
NM_002106.3:c.21A= NP_002097.1:p.Gly7=
NM_002106.4:c.21A= MANE Select NP_002097.1:p.Gly7=