LDH info

Canonical Allele Identifier: CA10576148
Gene: PTGFR HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 225991
ClinVar RCV Id: RCV000211367
dbSNP Id: rs3753380

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.78490747T>C , CM000663.2:g.78490747T>C GRCh38
NC_000001.10:g.78956432T>C , CM000663.1:g.78956432T>C GRCh37
NC_000001.9:g.78729020T>C NCBI36
NG_052997.1:g.4774T>C

Transcript Alleles

HGVS Amino-acid change
XM_006710781.2:c.-72-1925T>C XP_006710844.1:p.=
ENST00000370758.5:c.-72-1925T>C ENSP00000359794.1:p.=