Canonical Allele Identifier: CA173953

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 137944
• ClinVar RCV Id: RCV000148005 ; RCV000266678 ; RCV002316379 ; RCV003221815
• dbSNP Id: rs34961586
• ExAC: 2:145161492 C / G
• gnomAD v2: 2-145161492-C-G
• gnomAD v3: 2-144403925-C-G
• gnomAD v4: 2-144403925-C-G
• MyVariant Identifiers: chr2:g.145161492C>G (hg19) ; chr2:g.144403925C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403925C>G , CM000664.2:g.144403925C>G	GRCh38
NC_000002.11:g.145161492C>G , CM000664.1:g.145161492C>G	GRCh37
NC_000002.10:g.144877962C>G	NCBI36
NG_016431.1:g.121467G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*647G>C	ENSP00000508434.1:n.*647G>C
ENST00000440875.6:c.21G>C	ENSP00000475553.3:p.Gly7=
ENST00000627532.3:c.798G>C MANE Select	ENSP00000487174.1:p.Gly266=
ENST00000636026.2:c.798G>C	ENSP00000490776.1:p.Gly266=
ENST00000636179.1:n.767G>C
ENST00000636413.1:c.462G>C	ENSP00000490508.1:p.Gly154=
ENST00000636471.1:c.798G>C	ENSP00000490317.1:p.Gly266=
ENST00000636732.2:c.*515G>C	ENSP00000490175.1:n.*515G>C
ENST00000636820.1:n.898G>C
ENST00000637045.1:c.462G>C	ENSP00000490141.1:p.Gly154=
ENST00000637267.2:c.798G>C	ENSP00000490293.2:p.Gly266=
ENST00000637304.1:c.462G>C	ENSP00000490872.1:p.Gly154=
ENST00000638007.1:c.462G>C	ENSP00000490723.1:p.Gly154=
ENST00000638087.1:c.462G>C	ENSP00000490673.1:p.Gly154=
ENST00000638128.1:c.21G>C	ENSP00000490934.1:p.Gly7=
ENST00000675069.1:c.-133-5075G>C	ENSP00000502467.1:n.-133-5075G>C
ENST00000303660.8:c.795G>C	ENSP00000302501.4:p.Gly265=
ENST00000392861.6:c.882G>C	ENSP00000376601.3:p.Gly294=
ENST00000409487.7:c.798G>C	ENSP00000386854.2:p.Gly266=
ENST00000419938.5:c.537G>C	ENSP00000394777.2:p.Gly179=
ENST00000427902.5:c.885G>C	ENSP00000395496.2:p.Gly295=
ENST00000440875.5:c.783G>C	ENSP00000475553.2:p.Gly261=
ENST00000539609.7:c.726G>C	ENSP00000443792.2:p.Gly242=
ENST00000558170.6:c.798G>C	ENSP00000454157.1:p.Gly266=
ENST00000627532.2:c.798G>C	ENSP00000487174.1:p.Gly266=
NM_001171653.1:c.726G>C	NP_001165124.1:p.Gly242=
NM_014795.3:c.798G>C	NP_055610.1:p.Gly266=
XM_006712881.2:c.798G>C	XP_006712944.1:p.Gly266=
XM_006712882.2:c.798G>C	XP_006712945.1:p.Gly266=
XM_011512231.1:c.789G>C	XP_011510533.1:p.Gly263=
XM_011512232.1:c.777G>C	XP_011510534.1:p.Gly259=
NM_014795.4:c.798G>C MANE Select	NP_055610.1:p.Gly266=
NM_001171653.2:c.726G>C	NP_001165124.1:p.Gly242=