LDH info

Canonical Allele Identifier: CA216970
Gene: KRT14 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14616
dbSNP Id: rs60725382

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584410A>T , CM000679.2:g.41584410A>T GRCh38
NC_000017.10:g.39740662A>T , CM000679.1:g.39740662A>T GRCh37
NC_000017.9:g.36994188A>T NCBI36
NG_008624.1:g.7486T>A

Transcript Alleles

HGVS Amino-acid change
NM_000526.4:c.612T>A VV NP_000517.2:p.Tyr204Ter
NM_000526.5:c.612T>A VV MANE Preferred NP_000517.3:p.Tyr204Ter
ENST00000167586.6:c.612T>A ENSP00000167586.6:p.Tyr204Ter
ENST00000476662.1:n.62T>A