LDH info

Canonical Allele Identifier: CA065105
Gene: WT1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 261713
dbSNP Id: rs2234583

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.32434752G>A , CM000673.2:g.32434752G>A GRCh38
NC_000011.9:g.32456298G>A , CM000673.1:g.32456298G>A GRCh37
NC_000011.8:g.32412874G>A NCBI36
NG_009272.1:g.5790C>T , LRG_525:g.5790C>T

Transcript Alleles

HGVS Amino-acid change
NM_000378.4:c.594C>T VV NP_000369.3:p.Asn198=
NM_024424.3:c.594C>T VV NP_077742.2:p.Asn198=
NM_024426.4:c.594C>T VV NP_077744.3:p.Asn198=
NM_000378.5:c.609C>T VV NP_000369.4:p.Asn203=
NM_024424.4:c.609C>T VV NP_077742.3:p.Asn203=
NM_024426.5:c.609C>T VV NP_077744.4:p.Asn203=
NR_160306.1:n.788C>T
ENST00000332351.7:c.594C>T ENSP00000331327.3:p.Asn198=
ENST00000379077.7:c.594C>T ENSP00000368368.3:p.Asn198=
ENST00000448076.7:c.594C>T ENSP00000413452.3:p.Asn198=
ENST00000452863.7:n.594C>T ENSP00000415516.3:p.Asn198=