LDH info

Canonical Allele Identifier: CA208386872
Gene: SIRT1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4746720

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67917073T>C , CM000672.2:g.67917073T>C GRCh38
NC_000010.10:g.69676830T>C , CM000672.1:g.69676830T>C GRCh37
NC_000010.9:g.69346836T>C NCBI36
NG_050664.1:g.37412T>C

Transcript Alleles

HGVS Amino-acid change
NM_001142498.1:c.*480T>C VV NP_001135970.1:p.=
NM_001314049.1:c.*480T>C VV NP_001300978.1:p.=
NM_012238.4:c.*480T>C VV NP_036370.2:p.=
XM_006717737.2:c.*480T>C XP_006717800.1:p.=
XM_011539561.1:c.*480T>C XP_011537863.1:p.=
NM_012238.5:c.*480T>C VV MANE Preferred NP_036370.2:p.=
ENST00000212015.10:c.*480T>C ENSP00000212015.6:p.=
ENST00000403579.1:c.*480T>C ENSP00000384063.1:p.=
ENST00000406900.5:c.*480T>C ENSP00000384508.1:p.=
ENST00000432464.5:c.*480T>C ENSP00000409208.1:p.=