Canonical Allele Identifier: CA348708471

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 574367
• ClinVar RCV Id: RCV000696287
• dbSNP Id: rs1560606278
• MyVariant Identifiers: chr2:g.145156400G>C (hg19) ; chr2:g.144398833G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398833G>C , CM000664.2:g.144398833G>C	GRCh38
NC_000002.11:g.145156400G>C , CM000664.1:g.145156400G>C	GRCh37
NC_000002.10:g.144872870G>C	NCBI36
NG_016431.1:g.126559C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2203C>G	ENSP00000508434.1:n.*2203C>G
ENST00000440875.6:c.1577C>G	ENSP00000475553.3:p.Pro526Arg
ENST00000627532.3:c.2354C>G MANE Select	ENSP00000487174.1:p.Pro785Arg
ENST00000636026.2:c.2354C>G	ENSP00000490776.1:p.Pro785Arg
ENST00000636179.1:n.2323C>G
ENST00000636413.1:c.2018C>G	ENSP00000490508.1:p.Pro673Arg
ENST00000636471.1:c.2429C>G	ENSP00000490317.1:p.Pro810Arg
ENST00000636732.2:c.*2071C>G	ENSP00000490175.1:n.*2071C>G
ENST00000636820.1:n.2454C>G
ENST00000637045.1:c.2018C>G	ENSP00000490141.1:p.Pro673Arg
ENST00000637304.1:c.2018C>G	ENSP00000490872.1:p.Pro673Arg
ENST00000638007.1:c.2018C>G	ENSP00000490723.1:p.Pro673Arg
ENST00000638087.1:c.2018C>G	ENSP00000490673.1:p.Pro673Arg
ENST00000638128.1:c.1577C>G	ENSP00000490934.1:p.Pro526Arg
ENST00000675069.1:c.-116C>G	ENSP00000502467.1:n.-116C>G
ENST00000675145.1:n.2902C>G
ENST00000303660.8:c.2351C>G	ENSP00000302501.4:p.Pro784Arg
ENST00000409487.7:c.2354C>G	ENSP00000386854.2:p.Pro785Arg
ENST00000419938.5:c.655+2366C>G	ENSP00000394777.2:n.655+2366C>G
ENST00000440875.5:c.1167+704C>G	ENSP00000475553.2:n.1167+704C>G
ENST00000539609.7:c.2282C>G	ENSP00000443792.2:p.Pro761Arg
ENST00000558170.6:c.2354C>G	ENSP00000454157.1:p.Pro785Arg
ENST00000627532.2:c.2354C>G	ENSP00000487174.1:p.Pro785Arg
NM_001171653.1:c.2282C>G	NP_001165124.1:p.Pro761Arg
NM_014795.3:c.2354C>G	NP_055610.1:p.Pro785Arg
XM_006712881.2:c.2354C>G	XP_006712944.1:p.Pro785Arg
XM_006712882.2:c.2354C>G	XP_006712945.1:p.Pro785Arg
XM_011512231.1:c.2345C>G	XP_011510533.1:p.Pro782Arg
XM_011512232.1:c.2333C>G	XP_011510534.1:p.Pro778Arg
NM_014795.4:c.2354C>G MANE Select	NP_055610.1:p.Pro785Arg
NM_001171653.2:c.2282C>G	NP_001165124.1:p.Pro761Arg