LDH info

Canonical Allele Identifier: CA114282
Gene: DPYD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 437
ClinVar RCV Id: RCV000000466
dbSNP Id: rs1801267

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.97098598C>T , CM000663.2:g.97098598C>T GRCh38
NC_000001.10:g.97564154C>T , CM000663.1:g.97564154C>T GRCh37
NC_000001.9:g.97336742C>T NCBI36
NG_008807.2:g.827462G>A , LRG_722:g.827462G>A

Transcript Alleles

HGVS Amino-acid change
NM_000110.3:c.2657G>A , LRG_722t1:c.2657G>A NP_000101.2:p.Arg886His
NR_046590.1:n.64+2612C>T
XM_005270562.3:c.2441G>A XP_005270619.2:p.Arg814His
XM_017000507.1:c.2546G>A XP_016855996.1:p.Arg849His
XM_017000508.2:c.2162G>A XP_016855997.1:p.Arg721His
XM_017000509.2:c.2162G>A XP_016855998.1:p.Arg721His
XM_017000510.1:c.2162G>A XP_016855999.1:p.Arg721His
ENST00000370192.7:c.2657G>A ENSP00000359211.3:p.Arg886His