Canonical Allele Identifier: CA553122448
Gene: H2AZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1303156633
gnomAD v2: 4-100870912-C-T
gnomAD v3: 4-99949755-C-T
gnomAD v4: 4-99949755-C-T
MyVariant Identifiers: chr4:g.100870912C>T (hg19) chr4:g.99949755C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949755C>T , CM000666.2:g.99949755C>T GRCh38
NC_000004.11:g.100870912C>T , CM000666.1:g.100870912C>T GRCh37
NC_000004.10:g.101089935C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.4-15G>A MANE Select ENSP00000296417.5:n.4-15G>A
ENST00000651623.1:c.4-15G>A ENSP00000498935.1:n.4-15G>A
ENST00000296417.5:c.4-15G>A ENSP00000296417.5:n.4-15G>A
ENST00000511203.1:n.545G>A
ENST00000511319.5:n.514G>A
ENST00000511348.1:n.189-15G>A
ENST00000527366.1:n.88-15G>A
ENST00000529158.5:n.53-15G>A
NM_002106.3:c.4-15G>A NP_002097.1:n.4-15G>A
NM_002106.4:c.4-15G>A MANE Select NP_002097.1:n.4-15G>A
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