Canonical Allele Identifier: CA272822
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 160320
ClinVar RCV Id: RCV000147995
dbSNP Id: rs587784564

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398858G>A , CM000664.2:g.144398858G>A GRCh38
NC_000002.11:g.145156425G>A , CM000664.1:g.145156425G>A GRCh37
NC_000002.10:g.144872895G>A NCBI36
NG_016431.1:g.126534C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2178C>T ENSP00000508434.1:n.*2178C>T
ENST00000440875.6:c.1552C>T ENSP00000475553.3:p.His518Tyr
ENST00000627532.3:c.2329C>T MANE Select ENSP00000487174.1:p.His777Tyr
ENST00000636026.2:c.2329C>T ENSP00000490776.1:p.His777Tyr
ENST00000636179.1:n.2298C>T
ENST00000636413.1:c.1993C>T ENSP00000490508.1:p.His665Tyr
ENST00000636471.1:c.2404C>T ENSP00000490317.1:p.His802Tyr
ENST00000636732.2:c.*2046C>T ENSP00000490175.1:n.*2046C>T
ENST00000636820.1:n.2429C>T
ENST00000637045.1:c.1993C>T ENSP00000490141.1:p.His665Tyr
ENST00000637304.1:c.1993C>T ENSP00000490872.1:p.His665Tyr
ENST00000638007.1:c.1993C>T ENSP00000490723.1:p.His665Tyr
ENST00000638087.1:c.1993C>T ENSP00000490673.1:p.His665Tyr
ENST00000638128.1:c.1552C>T ENSP00000490934.1:p.His518Tyr
ENST00000675069.1:c.-133-8C>T ENSP00000502467.1:n.-133-8C>T
ENST00000675145.1:n.2877C>T
ENST00000303660.8:c.2326C>T ENSP00000302501.4:p.His776Tyr
ENST00000409487.7:c.2329C>T ENSP00000386854.2:p.His777Tyr
ENST00000419938.5:c.655+2341C>T ENSP00000394777.2:n.655+2341C>T
ENST00000440875.5:c.1167+679C>T ENSP00000475553.2:n.1167+679C>T
ENST00000539609.7:c.2257C>T ENSP00000443792.2:p.His753Tyr
ENST00000558170.6:c.2329C>T ENSP00000454157.1:p.His777Tyr
ENST00000627532.2:c.2329C>T ENSP00000487174.1:p.His777Tyr
NM_001171653.1:c.2257C>T NP_001165124.1:p.His753Tyr
NM_014795.3:c.2329C>T NP_055610.1:p.His777Tyr
XM_006712881.2:c.2329C>T XP_006712944.1:p.His777Tyr
XM_006712882.2:c.2329C>T XP_006712945.1:p.His777Tyr
XM_011512231.1:c.2320C>T XP_011510533.1:p.His774Tyr
XM_011512232.1:c.2308C>T XP_011510534.1:p.His770Tyr
NM_014795.4:c.2329C>T MANE Select NP_055610.1:p.His777Tyr
NM_001171653.2:c.2257C>T NP_001165124.1:p.His753Tyr