Canonical Allele Identifier: CA274521
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 189279
ClinVar RCV Id: RCV000169713 RCV000224619
dbSNP Id: rs786204813
MyVariant Identifiers: chr2:g.145274844del (hg19) chr2:g.144517277del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144517278del , CM000664.2:g.144517278del GRCh38
NC_000002.11:g.145274845del , CM000664.1:g.145274845del GRCh37
NC_000002.10:g.144991315del NCBI36
NG_016431.1:g.8115del

Transcript Alleles

HGVS Amino-acid change
ENST00000637591.2:n.142+1del
ENST00000689298.1:c.73+1del
ENST00000627532.3:c.73+1del
ENST00000636026.2:c.73+1del
ENST00000636445.1:c.73+1del
ENST00000636471.1:c.73+1del
ENST00000636732.2:c.73+1del
ENST00000637267.2:c.73+1del
ENST00000637591.1:n.32+1del
ENST00000675069.1:c.-134+2875del ENSP00000502467.1:n.-134+2875del
ENST00000303660.8:c.73+1del
ENST00000392861.6:c.157+1del
ENST00000409211.5:c.73+1del
ENST00000409487.7:c.73+1del
ENST00000419938.5:c.73+1del
ENST00000427902.5:c.160+1del
ENST00000431672.4:c.73+1del
ENST00000434448.5:c.73+1del
ENST00000435831.5:c.73+1del
ENST00000440875.5:c.58+1del
ENST00000444559.5:c.73+1del
ENST00000453352.5:n.323+1del
ENST00000461784.3:n.280+1del
ENST00000462355.2:c.73+1del
ENST00000465070.5:c.73+1del
ENST00000465308.5:c.73+1del
ENST00000470879.5:c.160+1del
ENST00000472146.5:n.323+1del
ENST00000476394.5:n.177+1del
ENST00000484313.3:c.73+1del
ENST00000539609.7:c.73+1del
ENST00000558170.6:c.73+1del
ENST00000627532.2:c.73+1del
ENST00000629520.2:c.73+1del
ENST00000629955.1:n.463+1del
ENST00000630572.2:c.73+1del
NM_001171653.1:c.73+1del
NM_014795.3:c.73+1del
NR_033258.1:n.595+1del
XM_006712881.2:c.73+1del
XM_006712882.2:c.73+1del
XM_011512232.1:c.52+2662del XP_011510534.1:n.52+2662del
NM_014795.4:c.73+1del
NM_001171653.2:c.73+1del
NR_033258.2:n.323+1del
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