LDH info

Canonical Allele Identifier: CA117861
Gene: CLDN16 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 5928
ClinVar RCV Id: RCV000006291
dbSNP Id: rs104893723

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.190408314G>A , CM000665.2:g.190408314G>A GRCh38
NC_000003.11:g.190126103G>A , CM000665.1:g.190126103G>A GRCh37
NC_000003.10:g.191608797G>A NCBI36
NG_008149.1:g.25263G>A

Transcript Alleles

HGVS Amino-acid change
NM_006580.3:c.593G>A VV NP_006571.1:p.Gly198Asp
ENST00000264734.2:c.593G>A ENSP00000264734.2:p.Gly198Asp
ENST00000456423.1:n.325-1589G>A ENSP00000414136.1:p.=