Canonical Allele Identifier: CA274509
Gene: ZEB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 189269
ClinVar RCV Id: RCV000169702
dbSNP Id: rs111724246

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144404063G>C , CM000664.2:g.144404063G>C GRCh38
NC_000002.10:g.144878100G>C NCBI36
NC_000002.11:g.145161630G>C , CM000664.1:g.145161630G>C GRCh37
NG_016431.1:g.121329C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303660.8:c.657C>G ENSP00000302501.4:p.Tyr219Ter
ENST00000392861.6:c.744C>G ENSP00000376601.3:p.Tyr248Ter
ENST00000409487.7:c.660C>G ENSP00000386854.2:p.Tyr220Ter
ENST00000419938.5:c.399C>G ENSP00000394777.2:p.Tyr133Ter
ENST00000427902.5:c.747C>G ENSP00000395496.2:p.Tyr249Ter
ENST00000440875.5:c.645C>G ENSP00000475553.2:p.Tyr215Ter
ENST00000497268.1:n.606C>G
ENST00000539609.7:c.588C>G ENSP00000443792.2:p.Tyr196Ter
ENST00000558170.6:c.660C>G ENSP00000454157.1:p.Tyr220Ter
ENST00000627532.2:c.660C>G ENSP00000487174.1:p.Tyr220Ter
NM_001171653.1:c.588C>G NP_001165124.1:p.Tyr196Ter
NM_014795.3:c.660C>G NP_055610.1:p.Tyr220Ter
XM_006712881.2:c.660C>G XP_006712944.1:p.Tyr220Ter
XM_006712882.2:c.660C>G XP_006712945.1:p.Tyr220Ter
XM_011512231.1:c.651C>G XP_011510533.1:p.Tyr217Ter
XM_011512232.1:c.639C>G XP_011510534.1:p.Tyr213Ter