Canonical Allele Identifier: CA16194506
Gene: H2AZ1 HGNC NCBI

Linked Data

dbSNP Id: rs61203457
gnomAD v3: 4-99949025-T-C
gnomAD v4: 4-99949025-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99949025T>C , CM000666.2:g.99949025T>C GRCh38
NC_000004.11:g.100870182T>C , CM000666.1:g.100870182T>C GRCh37
NC_000004.10:g.101089205T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296417.6:c.196-85A>G MANE Select ENSP00000296417.5:n.196-85A>G
ENST00000651623.1:c.196-85A>G ENSP00000498935.1:n.196-85A>G
ENST00000296417.5:c.196-85A>G ENSP00000296417.5:n.196-85A>G
ENST00000511203.1:n.1028-85A>G
ENST00000511319.5:n.721-85A>G
ENST00000511348.1:n.904A>G
ENST00000527366.1:n.273-85A>G
ENST00000529158.5:n.245-85A>G
NM_002106.3:c.196-85A>G NP_002097.1:n.196-85A>G
NM_002106.4:c.196-85A>G MANE Select NP_002097.1:n.196-85A>G