LDH info

Canonical Allele Identifier: CA16510567
Gene: HYKK HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs8034191

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78513681T>C , CM000677.2:g.78513681T>C GRCh38
NC_000015.9:g.78806023T>C , CM000677.1:g.78806023T>C GRCh37
NC_000015.8:g.76593078T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001013619.2:c.337+256T>C VV NP_001013641.2:p.=
NM_001083612.1:c.337+256T>C VV NP_001077081.1:p.=
XM_011521231.1:c.337+256T>C XP_011519533.1:p.=
XR_243078.3:n.432+256T>C
NM_001013619.3:c.337+256T>C VV NP_001013641.2:p.=
NM_001013619.4:c.337+256T>C VV MANE Preferred NP_001013641.2:p.=
ENST00000388988.8:c.337+256T>C ENSP00000373640.4:p.=
ENST00000408962.6:c.337+256T>C ENSP00000386197.2:p.=
ENST00000563233.2:n.337+256T>C ENSP00000454850.1:p.=
ENST00000566289.5:c.337+256T>C ENSP00000456614.1:p.=
ENST00000566332.5:c.337+256T>C ENSP00000457154.1:p.=
ENST00000569878.5:n.337+256T>C ENSP00000455459.1:p.=