Canonical Allele Identifier: CA1037410136
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144386965C>A , CM000664.2:g.144386965C>A GRCh38
NC_000002.11:g.145144532C>A , CM000664.1:g.145144532C>A GRCh37
NC_000002.10:g.144861002C>A NCBI36
NG_016431.1:g.138427G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000627532.3:c.*2486G>T MANE Select ENSP00000487174.1:n.*2486G>T
ENST00000636179.1:n.6100G>T
ENST00000636413.1:c.*2486G>T ENSP00000490508.1:n.*2486G>T
ENST00000636471.1:c.*2486G>T ENSP00000490317.1:n.*2486G>T
ENST00000636820.1:n.6231G>T
ENST00000637045.1:c.*2486G>T ENSP00000490141.1:n.*2486G>T
ENST00000637304.1:c.*2486G>T ENSP00000490872.1:n.*2486G>T
ENST00000638007.1:c.*2486G>T ENSP00000490723.1:n.*2486G>T
ENST00000638087.1:c.*2486G>T ENSP00000490673.1:n.*2486G>T
ENST00000638128.1:c.*2486G>T ENSP00000490934.1:n.*2486G>T
ENST00000639389.1:c.151+9447G>T ENSP00000492572.1:n.151+9447G>T
ENST00000627532.2:c.*2486G>T ENSP00000487174.1:n.*2486G>T
NM_001171653.1:c.*2486G>T NP_001165124.1:n.*2486G>T
NM_014795.3:c.*2486G>T NP_055610.1:n.*2486G>T
XM_006712881.2:c.*2486G>T XP_006712944.1:n.*2486G>T
XM_006712882.2:c.*2486G>T XP_006712945.1:n.*2486G>T
XM_011512231.1:c.*2486G>T XP_011510533.1:n.*2486G>T
XM_011512232.1:c.*2486G>T XP_011510534.1:n.*2486G>T
NM_014795.4:c.*2486G>T MANE Select NP_055610.1:n.*2486G>T
NM_001171653.2:c.*2486G>T NP_001165124.1:n.*2486G>T