Canonical Allele Identifier: CA758235375

Gene: ZEB2

Linked Data

• dbSNP Id: rs1342115986
• gnomAD v3: 2-144388806-A-G
• gnomAD v4: 2-144388806-A-G
• MyVariant Identifiers: chr2:g.145146373A>G (hg19) ; chr2:g.144388806A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144388806A>G , CM000664.2:g.144388806A>G	GRCh38
NC_000002.11:g.145146373A>G , CM000664.1:g.145146373A>G	GRCh37
NC_000002.10:g.144862843A>G	NCBI36
NG_016431.1:g.136586T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440875.6:c.*645T>C	ENSP00000475553.3:n.*645T>C
ENST00000627532.3:c.*645T>C MANE Select	ENSP00000487174.1:n.*645T>C
ENST00000636026.2:c.*569T>C	ENSP00000490776.1:n.*569T>C
ENST00000636179.1:n.4259T>C
ENST00000636413.1:c.*645T>C	ENSP00000490508.1:n.*645T>C
ENST00000636471.1:c.*645T>C	ENSP00000490317.1:n.*645T>C
ENST00000636732.2:c.*4007T>C	ENSP00000490175.1:n.*4007T>C
ENST00000636820.1:n.4390T>C
ENST00000637045.1:c.*645T>C	ENSP00000490141.1:n.*645T>C
ENST00000637304.1:c.*645T>C	ENSP00000490872.1:n.*645T>C
ENST00000638007.1:c.*645T>C	ENSP00000490723.1:n.*645T>C
ENST00000638087.1:c.*645T>C	ENSP00000490673.1:n.*645T>C
ENST00000638128.1:c.*645T>C	ENSP00000490934.1:n.*645T>C
ENST00000639389.1:c.151+7606T>C	ENSP00000492572.1:n.151+7606T>C
ENST00000647488.1:c.1510T>C	ENSP00000494820.1:n.1510T>C
ENST00000675069.1:c.*645T>C	ENSP00000502467.1:n.*645T>C
ENST00000409487.7:c.*645T>C	ENSP00000386854.2:n.*645T>C
ENST00000419938.5:c.*69T>C	ENSP00000394777.2:n.*69T>C
ENST00000627532.2:c.*645T>C	ENSP00000487174.1:n.*645T>C
NM_001171653.1:c.*645T>C	NP_001165124.1:n.*645T>C
NM_014795.3:c.*645T>C	NP_055610.1:n.*645T>C
XM_006712881.2:c.*645T>C	XP_006712944.1:n.*645T>C
XM_006712882.2:c.*645T>C	XP_006712945.1:n.*645T>C
XM_011512231.1:c.*645T>C	XP_011510533.1:n.*645T>C
XM_011512232.1:c.*645T>C	XP_011510534.1:n.*645T>C
NM_014795.4:c.*645T>C MANE Select	NP_055610.1:n.*645T>C
NM_001171653.2:c.*645T>C	NP_001165124.1:n.*645T>C