Canonical Allele Identifier: CA429217456
Gene: ZEB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.145147054T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389487T>C , CM000664.2:g.144389487T>C GRCh38
NC_000002.11:g.145147054T>C , CM000664.1:g.145147054T>C GRCh37
NC_000002.10:g.144863524T>C NCBI36
NG_016431.1:g.135905A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3458A>G ENSP00000508434.1:n.*3458A>G
ENST00000440875.6:c.2832A>G ENSP00000475553.3:p.Ser944=
ENST00000627532.3:c.3609A>G MANE Select ENSP00000487174.1:p.Ser1203=
ENST00000636026.2:c.3497A>G ENSP00000490776.1:p.Gln1166Arg
ENST00000636179.1:n.3578A>G
ENST00000636413.1:c.3273A>G ENSP00000490508.1:p.Ser1091=
ENST00000636471.1:c.3684A>G ENSP00000490317.1:p.Ser1228=
ENST00000636732.2:c.*3326A>G ENSP00000490175.1:n.*3326A>G
ENST00000636820.1:n.3709A>G
ENST00000637045.1:c.3273A>G ENSP00000490141.1:p.Ser1091=
ENST00000637304.1:c.3273A>G ENSP00000490872.1:p.Ser1091=
ENST00000638007.1:c.3273A>G ENSP00000490723.1:p.Ser1091=
ENST00000638087.1:c.3273A>G ENSP00000490673.1:p.Ser1091=
ENST00000638128.1:c.2832A>G ENSP00000490934.1:p.Ser944=
ENST00000639389.1:c.151+6925A>G ENSP00000492572.1:n.151+6925A>G
ENST00000647488.1:c.829A>G ENSP00000494820.1:n.829A>G
ENST00000675069.1:c.1140A>G ENSP00000502467.1:p.Ser380=
ENST00000303660.8:c.3606A>G ENSP00000302501.4:p.Ser1202=
ENST00000409487.7:c.3609A>G ENSP00000386854.2:p.Ser1203=
ENST00000419938.5:c.656-605A>G ENSP00000394777.2:n.656-605A>G
ENST00000539609.7:c.3537A>G ENSP00000443792.2:p.Ser1179=
ENST00000558170.6:c.3609A>G ENSP00000454157.1:p.Ser1203=
ENST00000627532.2:c.3609A>G ENSP00000487174.1:p.Ser1203=
NM_001171653.1:c.3537A>G NP_001165124.1:p.Ser1179=
NM_014795.3:c.3609A>G NP_055610.1:p.Ser1203=
XM_006712881.2:c.3609A>G XP_006712944.1:p.Ser1203=
XM_006712882.2:c.3609A>G XP_006712945.1:p.Ser1203=
XM_011512231.1:c.3600A>G XP_011510533.1:p.Ser1200=
XM_011512232.1:c.3588A>G XP_011510534.1:p.Ser1196=
NM_014795.4:c.3609A>G MANE Select NP_055610.1:p.Ser1203=
NM_001171653.2:c.3537A>G NP_001165124.1:p.Ser1179=