Canonical Allele Identifier: CA3023641
Gene: H2AZ1 HGNC NCBI

Linked Data

dbSNP Id: rs200739517
ExAC: 4:100870910 C / A
gnomAD v2: 4-100870910-C-A
gnomAD v4: 4-99949753-C-A
MyVariant Identifiers: chr4:g.100870910C>A (hg19) chr4:g.99949753C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949753C>A , CM000666.2:g.99949753C>A GRCh38
NC_000004.11:g.100870910C>A , CM000666.1:g.100870910C>A GRCh37
NC_000004.10:g.101089933C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.4-13G>T MANE Select ENSP00000296417.5:n.4-13G>T
ENST00000651623.1:c.4-13G>T ENSP00000498935.1:n.4-13G>T
ENST00000296417.5:c.4-13G>T ENSP00000296417.5:n.4-13G>T
ENST00000511203.1:n.547G>T
ENST00000511319.5:n.516G>T
ENST00000511348.1:n.189-13G>T
ENST00000527366.1:n.88-13G>T
ENST00000529158.5:n.53-13G>T
NM_002106.3:c.4-13G>T NP_002097.1:n.4-13G>T
NM_002106.4:c.4-13G>T MANE Select NP_002097.1:n.4-13G>T
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Search 100 bp 3'