LDH info

Canonical Allele Identifier: CA130257

Identifiers and link-outs to other resources

ClinVar Variation Id: 5849
dbSNP Id: rs121908450

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929288C>T , CM000664.2:g.108929288C>T GRCh38
NC_000002.11:g.109545744C>T , CM000664.1:g.109545744C>T GRCh37
NC_000002.10:g.108912176C>T NCBI36
NG_008257.1:g.65085G>A

Transcript Alleles

HGVS Amino-acid change
NM_022336.3:c.266G>A (EDAR) VV NP_071731.1:p.Arg89His
XM_006712204.1:c.266G>A (EDAR) XP_006712267.1:p.Arg89His
XM_011510502.1:c.317G>A (EDAR) XP_011508804.1:p.Arg106His
XM_011510503.1:c.317G>A (EDAR) XP_011508805.1:p.Arg106His
XM_011510502.2:c.410G>A (EDAR) XP_011508804.2:p.Arg137His
XM_011510503.2:c.410G>A (EDAR) XP_011508805.2:p.Arg137His
XM_017004623.2:c.8370+156242C>T (RANBP2) XP_016860112.1:p.=
NM_022336.4:c.266G>A (EDAR) VV NP_071731.1:p.Arg89His
ENST00000258443.6:c.266G>A ENSP00000258443.2:p.Arg89His
ENST00000376651.1:c.266G>A ENSP00000365839.1:p.Arg89His
ENST00000409271.5:c.266G>A ENSP00000386371.1:p.Arg89His