LDH info

Canonical Allele Identifier: CA256818
Gene: TTR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13437
ClinVar RCV Id: RCV000014379
dbSNP Id: rs104894664

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592959G>A , CM000680.2:g.31592959G>A GRCh38
NC_000018.9:g.29172922G>A , CM000680.1:g.29172922G>A GRCh37
NC_000018.8:g.27426920G>A NCBI36
NG_009490.1:g.6193G>A , LRG_416:g.6193G>A

Transcript Alleles

HGVS Amino-acid change
NM_000371.3:c.133G>A , LRG_416t1:c.133G>A NP_000362.1:p.Ala45Thr
ENST00000237014.7:c.133G>A ENSP00000237014.3:p.Ala45Thr
ENST00000432547.7:n.159G>A
ENST00000541025.2:n.159G>A
ENST00000610404.4:c.133G>A ENSP00000477599.1:p.Ala45Thr
ENST00000613781.1:c.133G>A ENSP00000479174.1:p.Ala45Thr