Canonical Allele Identifier: CA348707020

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 2634043
• ClinVar RCV Id: RCV003400484
• dbSNP Id: rs1408659659
• MyVariant Identifiers: chr2:g.145155980C>G (hg19) ; chr2:g.144398413C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398413C>G , CM000664.2:g.144398413C>G	GRCh38
NC_000002.11:g.145155980C>G , CM000664.1:g.145155980C>G	GRCh37
NC_000002.10:g.144872450C>G	NCBI36
NG_016431.1:g.126979G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2623G>C	ENSP00000508434.1:n.*2623G>C
ENST00000440875.6:c.1997G>C	ENSP00000475553.3:p.Gly666Ala
ENST00000627532.3:c.2774G>C MANE Select	ENSP00000487174.1:p.Gly925Ala
ENST00000636026.2:c.2774G>C	ENSP00000490776.1:p.Gly925Ala
ENST00000636179.1:n.2743G>C
ENST00000636413.1:c.2438G>C	ENSP00000490508.1:p.Gly813Ala
ENST00000636471.1:c.2849G>C	ENSP00000490317.1:p.Gly950Ala
ENST00000636732.2:c.*2491G>C	ENSP00000490175.1:n.*2491G>C
ENST00000636820.1:n.2874G>C
ENST00000637045.1:c.2438G>C	ENSP00000490141.1:p.Gly813Ala
ENST00000637304.1:c.2438G>C	ENSP00000490872.1:p.Gly813Ala
ENST00000638007.1:c.2438G>C	ENSP00000490723.1:p.Gly813Ala
ENST00000638087.1:c.2438G>C	ENSP00000490673.1:p.Gly813Ala
ENST00000638128.1:c.1997G>C	ENSP00000490934.1:p.Gly666Ala
ENST00000675069.1:c.305G>C	ENSP00000502467.1:p.Gly102Ala
ENST00000303660.8:c.2771G>C	ENSP00000302501.4:p.Gly924Ala
ENST00000409487.7:c.2774G>C	ENSP00000386854.2:p.Gly925Ala
ENST00000419938.5:c.655+2786G>C	ENSP00000394777.2:n.655+2786G>C
ENST00000440875.5:c.1168-485G>C	ENSP00000475553.2:n.1168-485G>C
ENST00000539609.7:c.2702G>C	ENSP00000443792.2:p.Gly901Ala
ENST00000558170.6:c.2774G>C	ENSP00000454157.1:p.Gly925Ala
ENST00000627532.2:c.2774G>C	ENSP00000487174.1:p.Gly925Ala
NM_001171653.1:c.2702G>C	NP_001165124.1:p.Gly901Ala
NM_014795.3:c.2774G>C	NP_055610.1:p.Gly925Ala
XM_006712881.2:c.2774G>C	XP_006712944.1:p.Gly925Ala
XM_006712882.2:c.2774G>C	XP_006712945.1:p.Gly925Ala
XM_011512231.1:c.2765G>C	XP_011510533.1:p.Gly922Ala
XM_011512232.1:c.2753G>C	XP_011510534.1:p.Gly918Ala
NM_014795.4:c.2774G>C MANE Select	NP_055610.1:p.Gly925Ala
NM_001171653.2:c.2702G>C	NP_001165124.1:p.Gly901Ala