Canonical Allele Identifier: CA5475246

Gene: ZNF33B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.42632414A>T , CM000672.2:g.42632414A>T	GRCh38
NC_000010.10:g.43127862A>T , CM000672.1:g.43127862A>T	GRCh37
NC_000010.9:g.42447868A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006955.3:c.35T>A MANE Select	NP_008886.1:p.Val12Glu
ENST00000359467.8:c.35T>A MANE Select	ENSP00000352444.2:p.Val12Glu
NM_001305033.1:c.56T>A	NP_001291962.1:p.Val19Glu
NM_001305033.2:c.56T>A	NP_001291962.1:p.Val19Glu
NM_001305035.1:c.-379T>A	NP_001291964.1:n.-379T>A
NM_001305035.2:c.-379T>A	NP_001291964.1:n.-379T>A
NM_001305036.1:c.-307T>A	NP_001291965.1:n.-307T>A
NM_001305036.2:c.-307T>A	NP_001291965.1:n.-307T>A
NM_001305037.1:c.-259-390T>A	NP_001291966.1:n.-259-390T>A
NM_001305037.2:c.-259-390T>A	NP_001291966.1:n.-259-390T>A
NM_001305038.1:c.-379T>A	NP_001291967.1:n.-379T>A
NM_001305038.2:c.-379T>A	NP_001291967.1:n.-379T>A
NM_001305039.1:c.-384T>A	NP_001291968.1:n.-384T>A
NM_001305039.2:c.-384T>A	NP_001291968.1:n.-384T>A
NM_001305040.1:c.-460T>A	NP_001291969.1:n.-460T>A
NM_001305040.2:c.-460T>A	NP_001291969.1:n.-460T>A
NM_006955.1:c.35T>A	NP_008886.1:p.Val12Glu
NM_006955.2:c.35T>A	NP_008886.1:p.Val12Glu
NR_130948.1:n.443T>A
NR_130948.2:n.176T>A
NR_130949.1:n.418-390T>A
NR_130949.2:n.151-390T>A
NR_130950.1:n.418-390T>A
NR_130950.2:n.151-390T>A
NR_130951.1:n.365-390T>A
NR_130951.2:n.98-390T>A
ENST00000359467.7:c.35T>A	ENSP00000352444.2:p.Val12Glu
ENST00000476796.2:n.127T>A
ENST00000486187.5:n.134-390T>A
ENST00000493285.2:c.56T>A	ENSP00000479296.1:p.Val19Glu
ENST00000613419.4:c.35T>A	ENSP00000481265.1:p.Val12Glu
XM_006717964.2:c.77-390T>A	XP_006718027.2:n.77-390T>A
XM_006717965.2:c.77-390T>A	XP_006718028.2:n.77-390T>A
XM_011540141.1:c.-381T>A	XP_011538443.1:n.-381T>A