Canonical Allele Identifier: CA297615

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 181743
• ClinVar RCV Id: RCV000159483
• dbSNP Id: rs730881201
• MyVariant Identifiers: chr2:g.145156025A>G (hg19) ; chr2:g.144398458A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398458A>G , CM000664.2:g.144398458A>G	GRCh38
NC_000002.11:g.145156025A>G , CM000664.1:g.145156025A>G	GRCh37
NC_000002.10:g.144872495A>G	NCBI36
NG_016431.1:g.126934T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2578T>C	ENSP00000508434.1:n.*2578T>C
ENST00000440875.6:c.1952T>C	ENSP00000475553.3:p.Met651Thr
ENST00000627532.3:c.2729T>C MANE Select	ENSP00000487174.1:p.Met910Thr
ENST00000636026.2:c.2729T>C	ENSP00000490776.1:p.Met910Thr
ENST00000636179.1:n.2698T>C
ENST00000636413.1:c.2393T>C	ENSP00000490508.1:p.Met798Thr
ENST00000636471.1:c.2804T>C	ENSP00000490317.1:p.Met935Thr
ENST00000636732.2:c.*2446T>C	ENSP00000490175.1:n.*2446T>C
ENST00000636820.1:n.2829T>C
ENST00000637045.1:c.2393T>C	ENSP00000490141.1:p.Met798Thr
ENST00000637304.1:c.2393T>C	ENSP00000490872.1:p.Met798Thr
ENST00000638007.1:c.2393T>C	ENSP00000490723.1:p.Met798Thr
ENST00000638087.1:c.2393T>C	ENSP00000490673.1:p.Met798Thr
ENST00000638128.1:c.1952T>C	ENSP00000490934.1:p.Met651Thr
ENST00000675069.1:c.260T>C	ENSP00000502467.1:p.Met87Thr
ENST00000303660.8:c.2726T>C	ENSP00000302501.4:p.Met909Thr
ENST00000409487.7:c.2729T>C	ENSP00000386854.2:p.Met910Thr
ENST00000419938.5:c.655+2741T>C	ENSP00000394777.2:n.655+2741T>C
ENST00000440875.5:c.1168-530T>C	ENSP00000475553.2:n.1168-530T>C
ENST00000539609.7:c.2657T>C	ENSP00000443792.2:p.Met886Thr
ENST00000558170.6:c.2729T>C	ENSP00000454157.1:p.Met910Thr
ENST00000627532.2:c.2729T>C	ENSP00000487174.1:p.Met910Thr
NM_001171653.1:c.2657T>C	NP_001165124.1:p.Met886Thr
NM_014795.3:c.2729T>C	NP_055610.1:p.Met910Thr
XM_006712881.2:c.2729T>C	XP_006712944.1:p.Met910Thr
XM_006712882.2:c.2729T>C	XP_006712945.1:p.Met910Thr
XM_011512231.1:c.2720T>C	XP_011510533.1:p.Met907Thr
XM_011512232.1:c.2708T>C	XP_011510534.1:p.Met903Thr
NM_014795.4:c.2729T>C MANE Select	NP_055610.1:p.Met910Thr
NM_001171653.2:c.2657T>C	NP_001165124.1:p.Met886Thr