Canonical Allele Identifier: CA16042334
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373033
ClinVar RCV Id: RCV000413462
dbSNP Id: rs1057518156

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399087G>C , CM000664.2:g.144399087G>C GRCh38
NC_000002.11:g.145156654G>C , CM000664.1:g.145156654G>C GRCh37
NC_000002.10:g.144873124G>C NCBI36
NG_016431.1:g.126305C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*1949C>G ENSP00000508434.1:n.*1949C>G
ENST00000440875.6:c.1323C>G ENSP00000475553.3:p.Tyr441Ter
ENST00000627532.3:c.2100C>G MANE Select ENSP00000487174.1:p.Tyr700Ter
ENST00000636026.2:c.2100C>G ENSP00000490776.1:p.Tyr700Ter
ENST00000636179.1:n.2069C>G
ENST00000636413.1:c.1764C>G ENSP00000490508.1:p.Tyr588Ter
ENST00000636471.1:c.2175C>G ENSP00000490317.1:p.Tyr725Ter
ENST00000636732.2:c.*1817C>G ENSP00000490175.1:n.*1817C>G
ENST00000636820.1:n.2200C>G
ENST00000637045.1:c.1764C>G ENSP00000490141.1:p.Tyr588Ter
ENST00000637304.1:c.1764C>G ENSP00000490872.1:p.Tyr588Ter
ENST00000638007.1:c.1764C>G ENSP00000490723.1:p.Tyr588Ter
ENST00000638087.1:c.1764C>G ENSP00000490673.1:p.Tyr588Ter
ENST00000638128.1:c.1323C>G ENSP00000490934.1:p.Tyr441Ter
ENST00000675069.1:c.-133-237C>G ENSP00000502467.1:n.-133-237C>G
ENST00000675145.1:n.2648C>G
ENST00000303660.8:c.2097C>G ENSP00000302501.4:p.Tyr699Ter
ENST00000409487.7:c.2100C>G ENSP00000386854.2:p.Tyr700Ter
ENST00000419938.5:c.655+2112C>G ENSP00000394777.2:n.655+2112C>G
ENST00000427902.5:c.2187C>G ENSP00000395496.2:p.Tyr729Ter
ENST00000440875.5:c.1167+450C>G ENSP00000475553.2:n.1167+450C>G
ENST00000539609.7:c.2028C>G ENSP00000443792.2:p.Tyr676Ter
ENST00000558170.6:c.2100C>G ENSP00000454157.1:p.Tyr700Ter
ENST00000627532.2:c.2100C>G ENSP00000487174.1:p.Tyr700Ter
NM_001171653.1:c.2028C>G NP_001165124.1:p.Tyr676Ter
NM_014795.3:c.2100C>G NP_055610.1:p.Tyr700Ter
XM_006712881.2:c.2100C>G XP_006712944.1:p.Tyr700Ter
XM_006712882.2:c.2100C>G XP_006712945.1:p.Tyr700Ter
XM_011512231.1:c.2091C>G XP_011510533.1:p.Tyr697Ter
XM_011512232.1:c.2079C>G XP_011510534.1:p.Tyr693Ter
NM_014795.4:c.2100C>G MANE Select NP_055610.1:p.Tyr700Ter
NM_001171653.2:c.2028C>G NP_001165124.1:p.Tyr676Ter