Canonical Allele Identifier: CA1898094
Gene: ZEB2 HGNC NCBI

Linked Data

dbSNP Id: rs753328374

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389461T>C , CM000664.2:g.144389461T>C GRCh38
NC_000002.11:g.145147028T>C , CM000664.1:g.145147028T>C GRCh37
NC_000002.10:g.144863498T>C NCBI36
NG_016431.1:g.135931A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3484A>G ENSP00000508434.1:n.*3484A>G
ENST00000440875.6:c.2858A>G ENSP00000475553.3:p.Asp953Gly
ENST00000627532.3:c.3635A>G MANE Select ENSP00000487174.1:p.Asp1212Gly
ENST00000636026.2:c.3523A>G ENSP00000490776.1:p.Met1175Val
ENST00000636179.1:n.3604A>G
ENST00000636413.1:c.3299A>G ENSP00000490508.1:p.Asp1100Gly
ENST00000636471.1:c.3710A>G ENSP00000490317.1:p.Asp1237Gly
ENST00000636732.2:c.*3352A>G ENSP00000490175.1:n.*3352A>G
ENST00000636820.1:n.3735A>G
ENST00000637045.1:c.3299A>G ENSP00000490141.1:p.Asp1100Gly
ENST00000637304.1:c.3299A>G ENSP00000490872.1:p.Asp1100Gly
ENST00000638007.1:c.3299A>G ENSP00000490723.1:p.Asp1100Gly
ENST00000638087.1:c.3299A>G ENSP00000490673.1:p.Asp1100Gly
ENST00000638128.1:c.2858A>G ENSP00000490934.1:p.Asp953Gly
ENST00000639389.1:c.151+6951A>G ENSP00000492572.1:n.151+6951A>G
ENST00000647488.1:c.855A>G ENSP00000494820.1:n.855A>G
ENST00000675069.1:c.1166A>G ENSP00000502467.1:p.Asp389Gly
ENST00000303660.8:c.3632A>G ENSP00000302501.4:p.Asp1211Gly
ENST00000409487.7:c.3635A>G ENSP00000386854.2:p.Asp1212Gly
ENST00000419938.5:c.656-579A>G ENSP00000394777.2:n.656-579A>G
ENST00000539609.7:c.3563A>G ENSP00000443792.2:p.Asp1188Gly
ENST00000558170.6:c.3635A>G ENSP00000454157.1:p.Asp1212Gly
ENST00000627532.2:c.3635A>G ENSP00000487174.1:p.Asp1212Gly
NM_001171653.1:c.3563A>G NP_001165124.1:p.Asp1188Gly
NM_014795.3:c.3635A>G NP_055610.1:p.Asp1212Gly
XM_006712881.2:c.3635A>G XP_006712944.1:p.Asp1212Gly
XM_006712882.2:c.3635A>G XP_006712945.1:p.Asp1212Gly
XM_011512231.1:c.3626A>G XP_011510533.1:p.Asp1209Gly
XM_011512232.1:c.3614A>G XP_011510534.1:p.Asp1205Gly
NM_014795.4:c.3635A>G MANE Select NP_055610.1:p.Asp1212Gly
NM_001171653.2:c.3563A>G NP_001165124.1:p.Asp1188Gly