Canonical Allele Identifier: CA357517078
Gene: H2AZ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100870878T>G (hg19) chr4:g.99949721T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949721T>G , CM000666.2:g.99949721T>G GRCh38
NC_000004.11:g.100870878T>G , CM000666.1:g.100870878T>G GRCh37
NC_000004.10:g.101089901T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.23A>C MANE Select ENSP00000296417.5:p.Lys8Thr
ENST00000651623.1:c.23A>C ENSP00000498935.1:p.Lys8Thr
ENST00000296417.5:c.23A>C ENSP00000296417.5:p.Lys8Thr
ENST00000511203.1:n.579A>C
ENST00000511319.5:n.548A>C
ENST00000511348.1:n.208A>C
ENST00000527366.1:n.107A>C
ENST00000529158.5:n.72A>C
NM_002106.3:c.23A>C NP_002097.1:p.Lys8Thr
NM_002106.4:c.23A>C MANE Select NP_002097.1:p.Lys8Thr
Search 100 bp 5'
Search 100 bp 3'