Canonical Allele Identifier: CA5474991
Gene: ZNF33B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.42593748G>A , CM000672.2:g.42593748G>A GRCh38
NC_000010.10:g.43089196G>A , CM000672.1:g.43089196G>A GRCh37
NC_000010.9:g.42409202G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006955.3:c.1202C>T MANE Select NP_008886.1:p.Thr401Ile
ENST00000359467.8:c.1202C>T MANE Select ENSP00000352444.2:p.Thr401Ile
NM_001305033.1:c.1223C>T NP_001291962.1:p.Thr408Ile
NM_001305033.2:c.1223C>T NP_001291962.1:p.Thr408Ile
NM_001305035.1:c.866C>T NP_001291964.1:p.Thr289Ile
NM_001305035.2:c.866C>T NP_001291964.1:p.Thr289Ile
NM_001305036.1:c.866C>T NP_001291965.1:p.Thr289Ile
NM_001305036.2:c.866C>T NP_001291965.1:p.Thr289Ile
NM_001305037.1:c.866C>T NP_001291966.1:p.Thr289Ile
NM_001305037.2:c.866C>T NP_001291966.1:p.Thr289Ile
NM_001305038.1:c.866C>T NP_001291967.1:p.Thr289Ile
NM_001305038.2:c.866C>T NP_001291967.1:p.Thr289Ile
NM_001305039.1:c.866C>T NP_001291968.1:p.Thr289Ile
NM_001305039.2:c.866C>T NP_001291968.1:p.Thr289Ile
NM_001305040.1:c.866C>T NP_001291969.1:p.Thr289Ile
NM_001305040.2:c.866C>T NP_001291969.1:p.Thr289Ile
NM_006955.1:c.1202C>T NP_008886.1:p.Thr401Ile
NM_006955.2:c.1202C>T NP_008886.1:p.Thr401Ile
NR_130948.1:n.763+847C>T
NR_130948.2:n.496+847C>T
NR_130949.1:n.695+847C>T
NR_130949.2:n.428+847C>T
NR_130950.1:n.615+847C>T
NR_130950.2:n.348+847C>T
NR_130951.1:n.565+847C>T
NR_130951.2:n.298+847C>T
ENST00000359467.7:c.1202C>T ENSP00000352444.2:p.Thr401Ile
ENST00000462075.1:c.73+847C>T ENSP00000484085.1:n.73+847C>T
ENST00000465206.5:c.274+847C>T ENSP00000480979.1:n.274+847C>T
ENST00000486187.5:n.411+847C>T
ENST00000613419.4:c.1202C>T ENSP00000481265.1:p.Thr401Ile
XM_006717964.2:c.1124C>T XP_006718027.2:p.Thr375Ile
XM_006717965.2:c.1121C>T XP_006718028.2:p.Thr374Ile
XM_011540141.1:c.866C>T XP_011538443.1:p.Thr289Ile
XM_011540142.1:c.866C>T XP_011538444.1:p.Thr289Ile