LDH info

Canonical Allele Identifier: CA123235
Gene: ITGB3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13558
dbSNP Id: rs5918

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47283364T>C , CM000679.2:g.47283364T>C GRCh38
NC_000017.10:g.45360730T>C , CM000679.1:g.45360730T>C GRCh37
NC_000017.9:g.42715729T>C NCBI36
NG_008332.2:g.34523T>C , LRG_481:g.34523T>C

Transcript Alleles

HGVS Amino-acid change
NM_000212.2:c.176T>C , LRG_481t1:c.176T>C NP_000203.2:p.Leu59Pro
NM_000212.3:c.176T>C VV MANE Preferred NP_000203.2:p.Leu59Pro
ENST00000559488.5:c.176T>C ENSP00000452786.1:p.Leu59Pro
ENST00000560629.1:n.141T>C
ENST00000571680.1:c.176T>C ENSP00000461626.1:p.Leu59Pro