Canonical Allele Identifier: CA348699066
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 574191
ClinVar RCV Id: RCV000696058
dbSNP Id: rs1238900874

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389560A>G , CM000664.2:g.144389560A>G GRCh38
NC_000002.11:g.145147127A>G , CM000664.1:g.145147127A>G GRCh37
NC_000002.10:g.144863597A>G NCBI36
NG_016431.1:g.135832T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3385T>C ENSP00000508434.1:n.*3385T>C
ENST00000440875.6:c.2759T>C ENSP00000475553.3:p.Ile920Thr
ENST00000627532.3:c.3536T>C MANE Select ENSP00000487174.1:p.Ile1179Thr
ENST00000636026.2:c.3424T>C ENSP00000490776.1:p.Tyr1142His
ENST00000636179.1:n.3505T>C
ENST00000636413.1:c.3200T>C ENSP00000490508.1:p.Ile1067Thr
ENST00000636471.1:c.3611T>C ENSP00000490317.1:p.Ile1204Thr
ENST00000636732.2:c.*3253T>C ENSP00000490175.1:n.*3253T>C
ENST00000636820.1:n.3636T>C
ENST00000637045.1:c.3200T>C ENSP00000490141.1:p.Ile1067Thr
ENST00000637304.1:c.3200T>C ENSP00000490872.1:p.Ile1067Thr
ENST00000638007.1:c.3200T>C ENSP00000490723.1:p.Ile1067Thr
ENST00000638087.1:c.3200T>C ENSP00000490673.1:p.Ile1067Thr
ENST00000638128.1:c.2759T>C ENSP00000490934.1:p.Ile920Thr
ENST00000639389.1:c.151+6852T>C ENSP00000492572.1:n.151+6852T>C
ENST00000647488.1:c.756T>C ENSP00000494820.1:n.756T>C
ENST00000675069.1:c.1067T>C ENSP00000502467.1:p.Ile356Thr
ENST00000303660.8:c.3533T>C ENSP00000302501.4:p.Ile1178Thr
ENST00000409487.7:c.3536T>C ENSP00000386854.2:p.Ile1179Thr
ENST00000419938.5:c.656-678T>C ENSP00000394777.2:n.656-678T>C
ENST00000539609.7:c.3464T>C ENSP00000443792.2:p.Ile1155Thr
ENST00000558170.6:c.3536T>C ENSP00000454157.1:p.Ile1179Thr
ENST00000627532.2:c.3536T>C ENSP00000487174.1:p.Ile1179Thr
NM_001171653.1:c.3464T>C NP_001165124.1:p.Ile1155Thr
NM_014795.3:c.3536T>C NP_055610.1:p.Ile1179Thr
XM_006712881.2:c.3536T>C XP_006712944.1:p.Ile1179Thr
XM_006712882.2:c.3536T>C XP_006712945.1:p.Ile1179Thr
XM_011512231.1:c.3527T>C XP_011510533.1:p.Ile1176Thr
XM_011512232.1:c.3515T>C XP_011510534.1:p.Ile1172Thr
NM_014795.4:c.3536T>C MANE Select NP_055610.1:p.Ile1179Thr
NM_001171653.2:c.3464T>C NP_001165124.1:p.Ile1155Thr