LDH info

Canonical Allele Identifier: CA117864
Gene: CLDN16 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 5931
dbSNP Id: rs104893726

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408416T>G , CM000665.2:g.190408416T>G GRCh38
NC_000003.11:g.190126205T>G , CM000665.1:g.190126205T>G GRCh37
NC_000003.10:g.191608899T>G NCBI36
NG_008149.1:g.25365T>G

Transcript Alleles

HGVS Amino-acid change
NM_006580.3:c.695T>G VV NP_006571.1:p.Phe232Cys
ENST00000264734.2:c.695T>G ENSP00000264734.2:p.Phe232Cys
ENST00000456423.1:n.325-1487T>G ENSP00000414136.1:p.=