Canonical Allele Identifier: CA5475251
Gene: ZNF33B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.42632435T>C , CM000672.2:g.42632435T>C GRCh38
NC_000010.10:g.43127883T>C , CM000672.1:g.43127883T>C GRCh37
NC_000010.9:g.42447889T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359467.8:c.14A>G MANE Select ENSP00000352444.2:p.Asp5Gly
ENST00000359467.7:c.14A>G ENSP00000352444.2:p.Asp5Gly
ENST00000476796.2:n.106A>G
ENST00000486187.5:n.134-411A>G
ENST00000493285.2:c.35A>G ENSP00000479296.1:p.Asp12Gly
ENST00000613419.4:c.14A>G ENSP00000481265.1:p.Asp5Gly
NM_001305033.1:c.35A>G NP_001291962.1:p.Asp12Gly
NM_001305035.1:c.-400A>G NP_001291964.1:n.-400A>G
NM_001305036.1:c.-328A>G NP_001291965.1:n.-328A>G
NM_001305037.1:c.-259-411A>G NP_001291966.1:n.-259-411A>G
NM_001305038.1:c.-400A>G NP_001291967.1:n.-400A>G
NM_001305039.1:c.-405A>G NP_001291968.1:n.-405A>G
NM_001305040.1:c.-481A>G NP_001291969.1:n.-481A>G
NM_006955.1:c.14A>G NP_008886.1:p.Asp5Gly
NM_006955.2:c.14A>G NP_008886.1:p.Asp5Gly
NR_130948.1:n.422A>G
NR_130949.1:n.418-411A>G
NR_130950.1:n.418-411A>G
NR_130951.1:n.365-411A>G
XM_006717964.2:c.77-411A>G XP_006718027.2:n.77-411A>G
XM_006717965.2:c.77-411A>G XP_006718028.2:n.77-411A>G
XM_011540141.1:c.-402A>G XP_011538443.1:n.-402A>G
NM_006955.3:c.14A>G MANE Select NP_008886.1:p.Asp5Gly
NM_001305033.2:c.35A>G NP_001291962.1:p.Asp12Gly
NM_001305035.2:c.-400A>G NP_001291964.1:n.-400A>G
NM_001305036.2:c.-328A>G NP_001291965.1:n.-328A>G
NM_001305037.2:c.-259-411A>G NP_001291966.1:n.-259-411A>G
NM_001305038.2:c.-400A>G NP_001291967.1:n.-400A>G
NM_001305039.2:c.-405A>G NP_001291968.1:n.-405A>G
NM_001305040.2:c.-481A>G NP_001291969.1:n.-481A>G
NR_130951.2:n.98-411A>G
NR_130948.2:n.155A>G
NR_130949.2:n.151-411A>G
NR_130950.2:n.151-411A>G