Canonical Allele Identifier: CA5475173

Gene: ZNF33B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.42594688C>T , CM000672.2:g.42594688C>T	GRCh38
NC_000010.10:g.43090136C>T , CM000672.1:g.43090136C>T	GRCh37
NC_000010.9:g.42410142C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359467.8:c.262G>A MANE Select	ENSP00000352444.2:p.Ala88Thr
ENST00000359467.7:c.262G>A	ENSP00000352444.2:p.Ala88Thr
ENST00000465206.5:c.181G>A	ENSP00000480979.1:p.Ala61Thr
ENST00000486187.5:n.318G>A
ENST00000613419.4:c.262G>A	ENSP00000481265.1:p.Ala88Thr
NM_001305033.1:c.283G>A	NP_001291962.1:p.Ala95Thr
NM_001305035.1:c.-75G>A	NP_001291964.1:n.-75G>A
NM_001305036.1:c.-75G>A	NP_001291965.1:n.-75G>A
NM_001305037.1:c.-75G>A	NP_001291966.1:n.-75G>A
NM_001305038.1:c.-75G>A	NP_001291967.1:n.-75G>A
NM_001305039.1:c.-75G>A	NP_001291968.1:n.-75G>A
NM_001305040.1:c.-75G>A	NP_001291969.1:n.-75G>A
NM_006955.1:c.262G>A	NP_008886.1:p.Ala88Thr
NM_006955.2:c.262G>A	NP_008886.1:p.Ala88Thr
NR_130948.1:n.670G>A
NR_130949.1:n.602G>A
NR_130950.1:n.522G>A
NR_130951.1:n.472G>A
XM_006717964.2:c.184G>A	XP_006718027.2:p.Ala62Thr
XM_006717965.2:c.181G>A	XP_006718028.2:p.Ala61Thr
XM_011540141.1:c.-75G>A	XP_011538443.1:n.-75G>A
XM_011540142.1:c.-75G>A	XP_011538444.1:n.-75G>A
NM_006955.3:c.262G>A MANE Select	NP_008886.1:p.Ala88Thr
NM_001305033.2:c.283G>A	NP_001291962.1:p.Ala95Thr
NM_001305035.2:c.-75G>A	NP_001291964.1:n.-75G>A
NM_001305036.2:c.-75G>A	NP_001291965.1:n.-75G>A
NM_001305037.2:c.-75G>A	NP_001291966.1:n.-75G>A
NM_001305038.2:c.-75G>A	NP_001291967.1:n.-75G>A
NM_001305039.2:c.-75G>A	NP_001291968.1:n.-75G>A
NM_001305040.2:c.-75G>A	NP_001291969.1:n.-75G>A
NR_130951.2:n.205G>A
NR_130948.2:n.403G>A
NR_130949.2:n.335G>A
NR_130950.2:n.255G>A