Canonical Allele Identifier: CA3023587
Gene: H2AZ1 HGNC NCBI

Linked Data

dbSNP Id: rs771352023
ExAC: 4:100870663 G / T
gnomAD v2: 4-100870663-G-T
gnomAD v3: 4-99949506-G-T
gnomAD v4: 4-99949506-G-T
MyVariant Identifiers: chr4:g.100870663G>T (hg19) chr4:g.99949506G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949506G>T , CM000666.2:g.99949506G>T GRCh38
NC_000004.11:g.100870663G>T , CM000666.1:g.100870663G>T GRCh37
NC_000004.10:g.101089686G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.82-120C>A MANE Select ENSP00000296417.5:n.82-120C>A
ENST00000651623.1:c.82-120C>A ENSP00000498935.1:n.82-120C>A
ENST00000296417.5:c.82-120C>A ENSP00000296417.5:n.82-120C>A
ENST00000511203.1:n.794C>A
ENST00000511319.5:n.607-120C>A
ENST00000511348.1:n.423C>A
ENST00000527366.1:n.166-127C>A
ENST00000529158.5:n.131-120C>A
NM_002106.3:c.82-120C>A NP_002097.1:n.82-120C>A
NM_002106.4:c.82-120C>A MANE Select NP_002097.1:n.82-120C>A
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