Canonical Allele Identifier: CA758245981

Gene: ZEB2

Linked Data

• dbSNP Id: rs1334786669
• gnomAD v3: 2-144517223-C-G
• gnomAD v4: 2-144517223-C-G
• MyVariant Identifiers: chr2:g.145274790C>G (hg19) ; chr2:g.144517223C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144517223C>G , CM000664.2:g.144517223C>G	GRCh38
NC_000002.11:g.145274790C>G , CM000664.1:g.145274790C>G	GRCh37
NC_000002.10:g.144991260C>G	NCBI36
NG_016431.1:g.8169G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000637591.2:n.142+55G>C
ENST00000689298.1:c.73+55G>C	ENSP00000508434.1:n.73+55G>C
ENST00000627532.3:c.73+55G>C MANE Select	ENSP00000487174.1:n.73+55G>C
ENST00000636026.2:c.73+55G>C	ENSP00000490776.1:n.73+55G>C
ENST00000636445.1:c.73+55G>C	ENSP00000490851.1:n.73+55G>C
ENST00000636471.1:c.73+55G>C	ENSP00000490317.1:n.73+55G>C
ENST00000636732.2:c.73+55G>C	ENSP00000490175.1:n.73+55G>C
ENST00000637267.2:c.73+55G>C	ENSP00000490293.2:n.73+55G>C
ENST00000637591.1:n.32+55G>C
ENST00000675069.1:c.-134+2929G>C	ENSP00000502467.1:n.-134+2929G>C
ENST00000303660.8:c.73+55G>C	ENSP00000302501.4:n.73+55G>C
ENST00000392861.6:c.157+55G>C	ENSP00000376601.3:n.157+55G>C
ENST00000409211.5:c.73+55G>C	ENSP00000387256.2:n.73+55G>C
ENST00000409487.7:c.73+55G>C	ENSP00000386854.2:n.73+55G>C
ENST00000419938.5:c.73+55G>C	ENSP00000394777.2:n.73+55G>C
ENST00000427902.5:c.160+55G>C	ENSP00000395496.2:n.160+55G>C
ENST00000431672.4:c.73+55G>C	ENSP00000475267.2:n.73+55G>C
ENST00000434448.5:c.73+55G>C	ENSP00000487261.1:n.73+55G>C
ENST00000435831.5:c.73+55G>C	ENSP00000400993.1:n.73+55G>C
ENST00000440875.5:c.58+55G>C	ENSP00000475553.2:n.58+55G>C
ENST00000444559.5:c.73+55G>C	ENSP00000399451.1:n.73+55G>C
ENST00000453352.5:n.323+55G>C
ENST00000461784.3:n.280+55G>C
ENST00000462355.2:c.73+55G>C	ENSP00000475400.1:n.73+55G>C
ENST00000465070.5:c.73+55G>C	ENSP00000475502.1:n.73+55G>C
ENST00000465308.5:c.73+55G>C	ENSP00000487476.1:n.73+55G>C
ENST00000470879.5:c.160+55G>C	ENSP00000475329.2:n.160+55G>C
ENST00000472146.5:n.323+55G>C
ENST00000476394.5:n.177+55G>C
ENST00000484313.3:c.73+55G>C	ENSP00000486341.1:n.73+55G>C
ENST00000539609.7:c.73+55G>C	ENSP00000443792.2:n.73+55G>C
ENST00000558170.6:c.73+55G>C	ENSP00000454157.1:n.73+55G>C
ENST00000627532.2:c.73+55G>C	ENSP00000487174.1:n.73+55G>C
ENST00000629520.2:c.73+55G>C	ENSP00000486240.1:n.73+55G>C
ENST00000629955.1:n.463+55G>C
ENST00000630572.2:c.73+55G>C	ENSP00000486346.1:n.73+55G>C
NM_001171653.1:c.73+55G>C	NP_001165124.1:n.73+55G>C
NM_014795.3:c.73+55G>C	NP_055610.1:n.73+55G>C
NR_033258.1:n.595+55G>C
XM_006712881.2:c.73+55G>C	XP_006712944.1:n.73+55G>C
XM_006712882.2:c.73+55G>C	XP_006712945.1:n.73+55G>C
XM_011512232.1:c.52+2716G>C	XP_011510534.1:n.52+2716G>C
NM_014795.4:c.73+55G>C MANE Select	NP_055610.1:n.73+55G>C
NM_001171653.2:c.73+55G>C	NP_001165124.1:n.73+55G>C
NR_033258.2:n.323+55G>C