Canonical Allele Identifier: CA5474809

Gene: ZNF33B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.42592824G>C , CM000672.2:g.42592824G>C	GRCh38
NC_000010.10:g.43088272G>C , CM000672.1:g.43088272G>C	GRCh37
NC_000010.9:g.42408278G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359467.8:c.2126C>G MANE Select	ENSP00000352444.2:p.Thr709Arg
ENST00000359467.7:c.2126C>G	ENSP00000352444.2:p.Thr709Arg
ENST00000462075.1:c.73+1771C>G	ENSP00000484085.1:n.73+1771C>G
ENST00000465206.5:c.274+1771C>G	ENSP00000480979.1:n.274+1771C>G
ENST00000486187.5:n.411+1771C>G
ENST00000613419.4:c.2126C>G	ENSP00000481265.1:p.Thr709Arg
NM_001305033.1:c.2147C>G	NP_001291962.1:p.Thr716Arg
NM_001305035.1:c.1790C>G	NP_001291964.1:p.Thr597Arg
NM_001305036.1:c.1790C>G	NP_001291965.1:p.Thr597Arg
NM_001305037.1:c.1790C>G	NP_001291966.1:p.Thr597Arg
NM_001305038.1:c.1790C>G	NP_001291967.1:p.Thr597Arg
NM_001305039.1:c.1790C>G	NP_001291968.1:p.Thr597Arg
NM_001305040.1:c.1790C>G	NP_001291969.1:p.Thr597Arg
NM_006955.1:c.2126C>G	NP_008886.1:p.Thr709Arg
NM_006955.2:c.2126C>G	NP_008886.1:p.Thr709Arg
NR_130948.1:n.763+1771C>G
NR_130949.1:n.695+1771C>G
NR_130950.1:n.615+1771C>G
NR_130951.1:n.565+1771C>G
XM_006717964.2:c.2048C>G	XP_006718027.2:p.Thr683Arg
XM_006717965.2:c.2045C>G	XP_006718028.2:p.Thr682Arg
XM_011540141.1:c.1790C>G	XP_011538443.1:p.Thr597Arg
XM_011540142.1:c.1790C>G	XP_011538444.1:p.Thr597Arg
NM_006955.3:c.2126C>G MANE Select	NP_008886.1:p.Thr709Arg
NM_001305033.2:c.2147C>G	NP_001291962.1:p.Thr716Arg
NM_001305035.2:c.1790C>G	NP_001291964.1:p.Thr597Arg
NM_001305036.2:c.1790C>G	NP_001291965.1:p.Thr597Arg
NM_001305037.2:c.1790C>G	NP_001291966.1:p.Thr597Arg
NM_001305038.2:c.1790C>G	NP_001291967.1:p.Thr597Arg
NM_001305039.2:c.1790C>G	NP_001291968.1:p.Thr597Arg
NM_001305040.2:c.1790C>G	NP_001291969.1:p.Thr597Arg
NR_130951.2:n.298+1771C>G
NR_130948.2:n.496+1771C>G
NR_130949.2:n.428+1771C>G
NR_130950.2:n.348+1771C>G