Canonical Allele Identifier: CA429217439
Gene: ZEB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.145147018T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389451T>C , CM000664.2:g.144389451T>C GRCh38
NC_000002.11:g.145147018T>C , CM000664.1:g.145147018T>C GRCh37
NC_000002.10:g.144863488T>C NCBI36
NG_016431.1:g.135941A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3494A>G ENSP00000508434.1:n.*3494A>G
ENST00000440875.6:c.2868A>G ENSP00000475553.3:p.Ter956=
ENST00000627532.3:c.3645A>G MANE Select ENSP00000487174.1:p.Ter1215=
ENST00000636026.2:c.3533A>G ENSP00000490776.1:p.Asn1178Ser
ENST00000636179.1:n.3614A>G
ENST00000636413.1:c.3309A>G ENSP00000490508.1:p.Ter1103=
ENST00000636471.1:c.3720A>G ENSP00000490317.1:p.Ter1240=
ENST00000636732.2:c.*3362A>G ENSP00000490175.1:n.*3362A>G
ENST00000636820.1:n.3745A>G
ENST00000637045.1:c.3309A>G ENSP00000490141.1:p.Ter1103=
ENST00000637304.1:c.3309A>G ENSP00000490872.1:p.Ter1103=
ENST00000638007.1:c.3309A>G ENSP00000490723.1:p.Ter1103=
ENST00000638087.1:c.3309A>G ENSP00000490673.1:p.Ter1103=
ENST00000638128.1:c.2868A>G ENSP00000490934.1:p.Ter956=
ENST00000639389.1:c.151+6961A>G ENSP00000492572.1:n.151+6961A>G
ENST00000647488.1:c.865A>G ENSP00000494820.1:n.865A>G
ENST00000675069.1:c.1176A>G ENSP00000502467.1:p.Ter392=
ENST00000303660.8:c.3642A>G ENSP00000302501.4:p.Ter1214=
ENST00000409487.7:c.3645A>G ENSP00000386854.2:p.Ter1215=
ENST00000419938.5:c.656-569A>G ENSP00000394777.2:n.656-569A>G
ENST00000539609.7:c.3573A>G ENSP00000443792.2:p.Ter1191=
ENST00000558170.6:c.3645A>G ENSP00000454157.1:p.Ter1215=
ENST00000627532.2:c.3645A>G ENSP00000487174.1:p.Ter1215=
NM_001171653.1:c.3573A>G NP_001165124.1:p.Ter1191=
NM_014795.3:c.3645A>G NP_055610.1:p.Ter1215=
XM_006712881.2:c.3645A>G XP_006712944.1:p.Ter1215=
XM_006712882.2:c.3645A>G XP_006712945.1:p.Ter1215=
XM_011512231.1:c.3636A>G XP_011510533.1:p.Ter1212=
XM_011512232.1:c.3624A>G XP_011510534.1:p.Ter1208=
NM_014795.4:c.3645A>G MANE Select NP_055610.1:p.Ter1215=
NM_001171653.2:c.3573A>G NP_001165124.1:p.Ter1191=