Canonical Allele Identifier: CA348706815

Gene: ZEB2

Linked Data

• dbSNP Id: rs1184670118
• gnomAD v2: 2-145155942-T-C
• gnomAD v4: 2-144398375-T-C
• MyVariant Identifiers: chr2:g.145155942T>C (hg19) ; chr2:g.144398375T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398375T>C , CM000664.2:g.144398375T>C	GRCh38
NC_000002.11:g.145155942T>C , CM000664.1:g.145155942T>C	GRCh37
NC_000002.10:g.144872412T>C	NCBI36
NG_016431.1:g.127017A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2661A>G	ENSP00000508434.1:n.*2661A>G
ENST00000440875.6:c.2035A>G	ENSP00000475553.3:p.Thr679Ala
ENST00000627532.3:c.2812A>G MANE Select	ENSP00000487174.1:p.Thr938Ala
ENST00000636026.2:c.2812A>G	ENSP00000490776.1:p.Thr938Ala
ENST00000636179.1:n.2781A>G
ENST00000636413.1:c.2476A>G	ENSP00000490508.1:p.Thr826Ala
ENST00000636471.1:c.2887A>G	ENSP00000490317.1:p.Thr963Ala
ENST00000636732.2:c.*2529A>G	ENSP00000490175.1:n.*2529A>G
ENST00000636820.1:n.2912A>G
ENST00000637045.1:c.2476A>G	ENSP00000490141.1:p.Thr826Ala
ENST00000637304.1:c.2476A>G	ENSP00000490872.1:p.Thr826Ala
ENST00000638007.1:c.2476A>G	ENSP00000490723.1:p.Thr826Ala
ENST00000638087.1:c.2476A>G	ENSP00000490673.1:p.Thr826Ala
ENST00000638128.1:c.2035A>G	ENSP00000490934.1:p.Thr679Ala
ENST00000675069.1:c.343A>G	ENSP00000502467.1:p.Thr115Ala
ENST00000303660.8:c.2809A>G	ENSP00000302501.4:p.Thr937Ala
ENST00000409487.7:c.2812A>G	ENSP00000386854.2:p.Thr938Ala
ENST00000419938.5:c.655+2824A>G	ENSP00000394777.2:n.655+2824A>G
ENST00000440875.5:c.1168-447A>G	ENSP00000475553.2:n.1168-447A>G
ENST00000539609.7:c.2740A>G	ENSP00000443792.2:p.Thr914Ala
ENST00000558170.6:c.2812A>G	ENSP00000454157.1:p.Thr938Ala
ENST00000627532.2:c.2812A>G	ENSP00000487174.1:p.Thr938Ala
NM_001171653.1:c.2740A>G	NP_001165124.1:p.Thr914Ala
NM_014795.3:c.2812A>G	NP_055610.1:p.Thr938Ala
XM_006712881.2:c.2812A>G	XP_006712944.1:p.Thr938Ala
XM_006712882.2:c.2812A>G	XP_006712945.1:p.Thr938Ala
XM_011512231.1:c.2803A>G	XP_011510533.1:p.Thr935Ala
XM_011512232.1:c.2791A>G	XP_011510534.1:p.Thr931Ala
NM_014795.4:c.2812A>G MANE Select	NP_055610.1:p.Thr938Ala
NM_001171653.2:c.2740A>G	NP_001165124.1:p.Thr914Ala