Canonical Allele Identifier: CA440341321
Gene: H2AZ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100870895A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949738A>C , CM000666.2:g.99949738A>C GRCh38
NC_000004.11:g.100870895A>C , CM000666.1:g.100870895A>C GRCh37
NC_000004.10:g.101089918A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.6T>G MANE Select ENSP00000296417.5:p.Ala2=
ENST00000651623.1:c.6T>G ENSP00000498935.1:p.Ala2=
ENST00000296417.5:c.6T>G ENSP00000296417.5:p.Ala2=
ENST00000511203.1:n.562T>G
ENST00000511319.5:n.531T>G
ENST00000511348.1:n.191T>G
ENST00000527366.1:n.90T>G
ENST00000529158.5:n.55T>G
NM_002106.3:c.6T>G NP_002097.1:p.Ala2=
NM_002106.4:c.6T>G MANE Select NP_002097.1:p.Ala2=
Search 100 bp 5'
Search 100 bp 3'