LDH info

Canonical Allele Identifier: CA267217
Gene: ZEB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 95641
ClinVar RCV Id: RCV000081675
dbSNP Id: rs398124284

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144403918G>A , CM000664.2:g.144403918G>A GRCh38
NC_000002.11:g.145161485G>A , CM000664.1:g.145161485G>A GRCh37
NC_000002.10:g.144877955G>A NCBI36
NG_016431.1:g.121474C>T

Transcript Alleles

HGVS Amino-acid change
NM_001171653.1:c.733C>T VV NP_001165124.1:p.Gln245Ter
NM_014795.3:c.805C>T VV NP_055610.1:p.Gln269Ter
XM_006712881.2:c.805C>T XP_006712944.1:p.Gln269Ter
XM_006712882.2:c.805C>T XP_006712945.1:p.Gln269Ter
XM_011512231.1:c.796C>T XP_011510533.1:p.Gln266Ter
XM_011512232.1:c.784C>T XP_011510534.1:p.Gln262Ter
NM_014795.4:c.805C>T VV MANE Preferred NP_055610.1:p.Gln269Ter
ENST00000303660.8:c.802C>T ENSP00000302501.4:p.Gln268Ter
ENST00000392861.6:c.889C>T ENSP00000376601.3:p.Gln297Ter
ENST00000409487.7:c.805C>T ENSP00000386854.2:p.Gln269Ter
ENST00000419938.5:c.544C>T ENSP00000394777.2:p.Gln182Ter
ENST00000427902.5:c.892C>T ENSP00000395496.2:p.Gln298Ter
ENST00000440875.5:c.790C>T ENSP00000475553.2:p.Gln264Ter
ENST00000539609.7:c.733C>T ENSP00000443792.2:p.Gln245Ter
ENST00000558170.6:c.805C>T ENSP00000454157.1:p.Gln269Ter
ENST00000627532.2:c.805C>T ENSP00000487174.1:p.Gln269Ter