Canonical Allele Identifier: CA553122452
Gene: H2AZ1 HGNC NCBI

Linked Data

dbSNP Id: rs1010103746
gnomAD v2: 4-100870916-C-G
gnomAD v3: 4-99949759-C-G
gnomAD v4: 4-99949759-C-G
MyVariant Identifiers: chr4:g.100870916C>G (hg19) chr4:g.99949759C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949759C>G , CM000666.2:g.99949759C>G GRCh38
NC_000004.11:g.100870916C>G , CM000666.1:g.100870916C>G GRCh37
NC_000004.10:g.101089939C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296417.6:c.4-19G>C MANE Select ENSP00000296417.5:n.4-19G>C
ENST00000651623.1:c.4-19G>C ENSP00000498935.1:n.4-19G>C
ENST00000296417.5:c.4-19G>C ENSP00000296417.5:n.4-19G>C
ENST00000511203.1:n.541G>C
ENST00000511319.5:n.510G>C
ENST00000511348.1:n.189-19G>C
ENST00000527366.1:n.88-19G>C
ENST00000529158.5:n.53-19G>C
NM_002106.3:c.4-19G>C NP_002097.1:n.4-19G>C
NM_002106.4:c.4-19G>C MANE Select NP_002097.1:n.4-19G>C
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