Canonical Allele Identifier: CA758238683

Gene: ZEB2

Linked Data

• dbSNP Id: rs1437569224
• gnomAD v3: 2-144450567-C-G
• gnomAD v4: 2-144450567-C-G
• MyVariant Identifiers: chr2:g.145208134C>G (hg19) ; chr2:g.144450567C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144450567C>G , CM000664.2:g.144450567C>G	GRCh38
NC_000002.11:g.145208134C>G , CM000664.1:g.145208134C>G	GRCh37
NC_000002.10:g.144924604C>G	NCBI36
NG_016431.1:g.74825G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000637591.2:n.222+19852G>C
ENST00000689298.1:c.103-20541G>C	ENSP00000508434.1:n.103-20541G>C
ENST00000440875.6:c.-633+4485G>C	ENSP00000475553.3:n.-633+4485G>C
ENST00000627532.3:c.74-20541G>C MANE Select	ENSP00000487174.1:n.74-20541G>C
ENST00000636026.2:c.74-20541G>C	ENSP00000490776.1:n.74-20541G>C
ENST00000636179.1:n.43-20541G>C
ENST00000636471.1:c.74-20541G>C	ENSP00000490317.1:n.74-20541G>C
ENST00000636732.2:c.74-20541G>C	ENSP00000490175.1:n.74-20541G>C
ENST00000636820.1:n.174-20541G>C
ENST00000637045.1:c.-264+4485G>C	ENSP00000490141.1:n.-264+4485G>C
ENST00000637267.2:c.74-20541G>C	ENSP00000490293.2:n.74-20541G>C
ENST00000637304.1:c.-263-20541G>C	ENSP00000490872.1:n.-263-20541G>C
ENST00000638128.1:c.-632-20541G>C	ENSP00000490934.1:n.-632-20541G>C
ENST00000675069.1:c.-133-51717G>C	ENSP00000502467.1:n.-133-51717G>C
ENST00000303660.8:c.74-20541G>C	ENSP00000302501.4:n.74-20541G>C
ENST00000392861.6:c.158-20541G>C	ENSP00000376601.3:n.158-20541G>C
ENST00000409211.5:c.74-20541G>C	ENSP00000387256.2:n.74-20541G>C
ENST00000409487.7:c.74-20541G>C	ENSP00000386854.2:n.74-20541G>C
ENST00000419938.5:c.74-20541G>C	ENSP00000394777.2:n.74-20541G>C
ENST00000427902.5:c.161-20541G>C	ENSP00000395496.2:n.161-20541G>C
ENST00000431672.4:c.74-20541G>C	ENSP00000475267.2:n.74-20541G>C
ENST00000434448.5:c.*5-20541G>C	ENSP00000487261.1:n.*5-20541G>C
ENST00000435831.5:c.74-20541G>C	ENSP00000400993.1:n.74-20541G>C
ENST00000440875.5:c.59-20541G>C	ENSP00000475553.2:n.59-20541G>C
ENST00000444559.5:c.74-20541G>C	ENSP00000399451.1:n.74-20541G>C
ENST00000453352.5:n.381-20541G>C
ENST00000461784.3:n.281-20541G>C
ENST00000465308.5:c.74-20541G>C	ENSP00000487476.1:n.74-20541G>C
ENST00000472146.5:n.324-20541G>C
ENST00000476394.5:n.178-20541G>C
ENST00000479735.1:n.305-20541G>C
ENST00000539609.7:c.74-20541G>C	ENSP00000443792.2:n.74-20541G>C
ENST00000558170.6:c.74-20541G>C	ENSP00000454157.1:n.74-20541G>C
ENST00000627532.2:c.74-20541G>C	ENSP00000487174.1:n.74-20541G>C
ENST00000630572.2:c.74-20541G>C	ENSP00000486346.1:n.74-20541G>C
NM_001171653.1:c.74-20541G>C	NP_001165124.1:n.74-20541G>C
NM_014795.3:c.74-20541G>C	NP_055610.1:n.74-20541G>C
XM_006712881.2:c.74-20541G>C	XP_006712944.1:n.74-20541G>C
XM_006712882.2:c.74-20541G>C	XP_006712945.1:n.74-20541G>C
XM_011512232.1:c.53-20541G>C	XP_011510534.1:n.53-20541G>C
XR_923405.1:n.5993C>G
XR_923406.1:n.5869C>G
XR_923407.1:n.5832C>G
XR_923408.1:n.5871C>G
XR_923409.1:n.5324C>G
NM_014795.4:c.74-20541G>C MANE Select	NP_055610.1:n.74-20541G>C
NM_001171653.2:c.74-20541G>C	NP_001165124.1:n.74-20541G>C