Canonical Allele Identifier: CA357516965
Gene: H2AZ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100870854T>G (hg19) chr4:g.99949697T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949697T>G , CM000666.2:g.99949697T>G GRCh38
NC_000004.11:g.100870854T>G , CM000666.1:g.100870854T>G GRCh37
NC_000004.10:g.101089877T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296417.6:c.47A>C MANE Select ENSP00000296417.5:p.Lys16Thr
ENST00000651623.1:c.47A>C ENSP00000498935.1:p.Lys16Thr
ENST00000296417.5:c.47A>C ENSP00000296417.5:p.Lys16Thr
ENST00000511203.1:n.603A>C
ENST00000511319.5:n.572A>C
ENST00000511348.1:n.232A>C
ENST00000527366.1:n.131A>C
ENST00000529158.5:n.96A>C
NM_002106.3:c.47A>C NP_002097.1:p.Lys16Thr
NM_002106.4:c.47A>C MANE Select NP_002097.1:p.Lys16Thr
Search 100 bp 5'
Search 100 bp 3'