Canonical Allele Identifier: CA102666188
Gene: H2AZ1 HGNC NCBI

Linked Data

dbSNP Id: rs899846176
gnomAD v2: 4-100870850-C-T
gnomAD v3: 4-99949693-C-T
gnomAD v4: 4-99949693-C-T
MyVariant Identifiers: chr4:g.100870850C>T (hg19) chr4:g.99949693C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949693C>T , CM000666.2:g.99949693C>T GRCh38
NC_000004.11:g.100870850C>T , CM000666.1:g.100870850C>T GRCh37
NC_000004.10:g.101089873C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.51G>A MANE Select ENSP00000296417.5:p.Ala17=
ENST00000651623.1:c.51G>A ENSP00000498935.1:p.Ala17=
ENST00000296417.5:c.51G>A ENSP00000296417.5:p.Ala17=
ENST00000511203.1:n.607G>A
ENST00000511319.5:n.576G>A
ENST00000511348.1:n.236G>A
ENST00000527366.1:n.135G>A
ENST00000529158.5:n.100G>A
NM_002106.3:c.51G>A NP_002097.1:p.Ala17=
NM_002106.4:c.51G>A MANE Select NP_002097.1:p.Ala17=
Search 100 bp 5'
Search 100 bp 3'