Canonical Allele Identifier: CA102666214
Gene: H2AZ1 HGNC NCBI

Linked Data

dbSNP Id: rs760644452
gnomAD v2: 4-100870892-G-A
gnomAD v3: 4-99949735-G-A
gnomAD v4: 4-99949735-G-A
MyVariant Identifiers: chr4:g.100870892G>A (hg19) chr4:g.99949735G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949735G>A , CM000666.2:g.99949735G>A GRCh38
NC_000004.11:g.100870892G>A , CM000666.1:g.100870892G>A GRCh37
NC_000004.10:g.101089915G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.9C>T MANE Select ENSP00000296417.5:p.Gly3=
ENST00000651623.1:c.9C>T ENSP00000498935.1:p.Gly3=
ENST00000296417.5:c.9C>T ENSP00000296417.5:p.Gly3=
ENST00000511203.1:n.565C>T
ENST00000511319.5:n.534C>T
ENST00000511348.1:n.194C>T
ENST00000527366.1:n.93C>T
ENST00000529158.5:n.58C>T
NM_002106.3:c.9C>T NP_002097.1:p.Gly3=
NM_002106.4:c.9C>T MANE Select NP_002097.1:p.Gly3=
Search 100 bp 5'
Search 100 bp 3'