Canonical Allele Identifier: CA267217
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95641
ClinVar RCV Id: RCV000081675
dbSNP Id: rs398124284
MyVariant Identifiers: chr2:g.145161485G>A (hg19) chr2:g.144403918G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144403918G>A , CM000664.2:g.144403918G>A GRCh38
NC_000002.11:g.145161485G>A , CM000664.1:g.145161485G>A GRCh37
NC_000002.10:g.144877955G>A NCBI36
NG_016431.1:g.121474C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*654C>T ENSP00000508434.1:n.*654C>T
ENST00000440875.6:c.28C>T ENSP00000475553.3:p.Gln10Ter
ENST00000627532.3:c.805C>T MANE Select ENSP00000487174.1:p.Gln269Ter
ENST00000636026.2:c.805C>T ENSP00000490776.1:p.Gln269Ter
ENST00000636179.1:n.774C>T
ENST00000636413.1:c.469C>T ENSP00000490508.1:p.Gln157Ter
ENST00000636471.1:c.805C>T ENSP00000490317.1:p.Gln269Ter
ENST00000636732.2:c.*522C>T ENSP00000490175.1:n.*522C>T
ENST00000636820.1:n.905C>T
ENST00000637045.1:c.469C>T ENSP00000490141.1:p.Gln157Ter
ENST00000637267.2:c.805C>T ENSP00000490293.2:p.Gln269Ter
ENST00000637304.1:c.469C>T ENSP00000490872.1:p.Gln157Ter
ENST00000638007.1:c.469C>T ENSP00000490723.1:p.Gln157Ter
ENST00000638087.1:c.469C>T ENSP00000490673.1:p.Gln157Ter
ENST00000638128.1:c.28C>T ENSP00000490934.1:p.Gln10Ter
ENST00000675069.1:c.-133-5068C>T ENSP00000502467.1:n.-133-5068C>T
ENST00000303660.8:c.802C>T ENSP00000302501.4:p.Gln268Ter
ENST00000392861.6:c.889C>T ENSP00000376601.3:p.Gln297Ter
ENST00000409487.7:c.805C>T ENSP00000386854.2:p.Gln269Ter
ENST00000419938.5:c.544C>T ENSP00000394777.2:p.Gln182Ter
ENST00000427902.5:c.892C>T ENSP00000395496.2:p.Gln298Ter
ENST00000440875.5:c.790C>T ENSP00000475553.2:p.Gln264Ter
ENST00000539609.7:c.733C>T ENSP00000443792.2:p.Gln245Ter
ENST00000558170.6:c.805C>T ENSP00000454157.1:p.Gln269Ter
ENST00000627532.2:c.805C>T ENSP00000487174.1:p.Gln269Ter
NM_001171653.1:c.733C>T NP_001165124.1:p.Gln245Ter
NM_014795.3:c.805C>T NP_055610.1:p.Gln269Ter
XM_006712881.2:c.805C>T XP_006712944.1:p.Gln269Ter
XM_006712882.2:c.805C>T XP_006712945.1:p.Gln269Ter
XM_011512231.1:c.796C>T XP_011510533.1:p.Gln266Ter
XM_011512232.1:c.784C>T XP_011510534.1:p.Gln262Ter
NM_014795.4:c.805C>T MANE Select NP_055610.1:p.Gln269Ter
NM_001171653.2:c.733C>T NP_001165124.1:p.Gln245Ter
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