Canonical Allele Identifier: CA348708510

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 661027
• ClinVar RCV Id: RCV000818354
• dbSNP Id: rs1573715809
• MyVariant Identifiers: chr2:g.145156417C>G (hg19) ; chr2:g.144398850C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398850C>G , CM000664.2:g.144398850C>G	GRCh38
NC_000002.11:g.145156417C>G , CM000664.1:g.145156417C>G	GRCh37
NC_000002.10:g.144872887C>G	NCBI36
NG_016431.1:g.126542G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2186G>C	ENSP00000508434.1:n.*2186G>C
ENST00000440875.6:c.1560G>C	ENSP00000475553.3:p.Arg520Ser
ENST00000627532.3:c.2337G>C MANE Select	ENSP00000487174.1:p.Arg779Ser
ENST00000636026.2:c.2337G>C	ENSP00000490776.1:p.Arg779Ser
ENST00000636179.1:n.2306G>C
ENST00000636413.1:c.2001G>C	ENSP00000490508.1:p.Arg667Ser
ENST00000636471.1:c.2412G>C	ENSP00000490317.1:p.Arg804Ser
ENST00000636732.2:c.*2054G>C	ENSP00000490175.1:n.*2054G>C
ENST00000636820.1:n.2437G>C
ENST00000637045.1:c.2001G>C	ENSP00000490141.1:p.Arg667Ser
ENST00000637304.1:c.2001G>C	ENSP00000490872.1:p.Arg667Ser
ENST00000638007.1:c.2001G>C	ENSP00000490723.1:p.Arg667Ser
ENST00000638087.1:c.2001G>C	ENSP00000490673.1:p.Arg667Ser
ENST00000638128.1:c.1560G>C	ENSP00000490934.1:p.Arg520Ser
ENST00000675069.1:c.-133G>C	ENSP00000502467.1:n.-133G>C
ENST00000675145.1:n.2885G>C
ENST00000303660.8:c.2334G>C	ENSP00000302501.4:p.Arg778Ser
ENST00000409487.7:c.2337G>C	ENSP00000386854.2:p.Arg779Ser
ENST00000419938.5:c.655+2349G>C	ENSP00000394777.2:n.655+2349G>C
ENST00000440875.5:c.1167+687G>C	ENSP00000475553.2:n.1167+687G>C
ENST00000539609.7:c.2265G>C	ENSP00000443792.2:p.Arg755Ser
ENST00000558170.6:c.2337G>C	ENSP00000454157.1:p.Arg779Ser
ENST00000627532.2:c.2337G>C	ENSP00000487174.1:p.Arg779Ser
NM_001171653.1:c.2265G>C	NP_001165124.1:p.Arg755Ser
NM_014795.3:c.2337G>C	NP_055610.1:p.Arg779Ser
XM_006712881.2:c.2337G>C	XP_006712944.1:p.Arg779Ser
XM_006712882.2:c.2337G>C	XP_006712945.1:p.Arg779Ser
XM_011512231.1:c.2328G>C	XP_011510533.1:p.Arg776Ser
XM_011512232.1:c.2316G>C	XP_011510534.1:p.Arg772Ser
NM_014795.4:c.2337G>C MANE Select	NP_055610.1:p.Arg779Ser
NM_001171653.2:c.2265G>C	NP_001165124.1:p.Arg755Ser