Canonical Allele Identifier: CA348699560

Gene: ZEB2

Linked Data

• dbSNP Id: rs1463669256
• gnomAD v2: 2-145147319-C-G
• gnomAD v4: 2-144389752-C-G
• MyVariant Identifiers: chr2:g.145147319C>G (hg19) ; chr2:g.144389752C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389752C>G , CM000664.2:g.144389752C>G	GRCh38
NC_000002.11:g.145147319C>G , CM000664.1:g.145147319C>G	GRCh37
NC_000002.10:g.144863789C>G	NCBI36
NG_016431.1:g.135640G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3193G>C	ENSP00000508434.1:n.*3193G>C
ENST00000440875.6:c.2567G>C	ENSP00000475553.3:p.Ser856Thr
ENST00000627532.3:c.3344G>C MANE Select	ENSP00000487174.1:p.Ser1115Thr
ENST00000636026.2:c.3232G>C	ENSP00000490776.1:p.Ala1078Pro
ENST00000636179.1:n.3313G>C
ENST00000636413.1:c.3008G>C	ENSP00000490508.1:p.Ser1003Thr
ENST00000636471.1:c.3419G>C	ENSP00000490317.1:p.Ser1140Thr
ENST00000636732.2:c.*3061G>C	ENSP00000490175.1:n.*3061G>C
ENST00000636820.1:n.3444G>C
ENST00000637045.1:c.3008G>C	ENSP00000490141.1:p.Ser1003Thr
ENST00000637304.1:c.3008G>C	ENSP00000490872.1:p.Ser1003Thr
ENST00000638007.1:c.3008G>C	ENSP00000490723.1:p.Ser1003Thr
ENST00000638087.1:c.3008G>C	ENSP00000490673.1:p.Ser1003Thr
ENST00000638128.1:c.2567G>C	ENSP00000490934.1:p.Ser856Thr
ENST00000639389.1:c.151+6660G>C	ENSP00000492572.1:n.151+6660G>C
ENST00000647488.1:c.564G>C	ENSP00000494820.1:n.564G>C
ENST00000675069.1:c.875G>C	ENSP00000502467.1:p.Ser292Thr
ENST00000303660.8:c.3341G>C	ENSP00000302501.4:p.Ser1114Thr
ENST00000409487.7:c.3344G>C	ENSP00000386854.2:p.Ser1115Thr
ENST00000419938.5:c.656-870G>C	ENSP00000394777.2:n.656-870G>C
ENST00000539609.7:c.3272G>C	ENSP00000443792.2:p.Ser1091Thr
ENST00000558170.6:c.3344G>C	ENSP00000454157.1:p.Ser1115Thr
ENST00000627532.2:c.3344G>C	ENSP00000487174.1:p.Ser1115Thr
NM_001171653.1:c.3272G>C	NP_001165124.1:p.Ser1091Thr
NM_014795.3:c.3344G>C	NP_055610.1:p.Ser1115Thr
XM_006712881.2:c.3344G>C	XP_006712944.1:p.Ser1115Thr
XM_006712882.2:c.3344G>C	XP_006712945.1:p.Ser1115Thr
XM_011512231.1:c.3335G>C	XP_011510533.1:p.Ser1112Thr
XM_011512232.1:c.3323G>C	XP_011510534.1:p.Ser1108Thr
NM_014795.4:c.3344G>C MANE Select	NP_055610.1:p.Ser1115Thr
NM_001171653.2:c.3272G>C	NP_001165124.1:p.Ser1091Thr