LDH info

Canonical Allele Identifier: CA15583079
Gene: SLC30A8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2466293

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117173699A>G , CM000670.2:g.117173699A>G GRCh38
NC_000008.10:g.118185938A>G , CM000670.1:g.118185938A>G GRCh37
NC_000008.9:g.118255119A>G NCBI36
NG_016991.1:g.228427A>G

Transcript Alleles

HGVS Amino-acid change
NM_001172811.1:c.*1018A>G VV NP_001166282.1:p.=
NM_001172813.1:c.*1018A>G VV NP_001166284.1:p.=
NM_001172814.1:c.*1018A>G VV NP_001166285.1:p.=
NM_001172815.1:c.*1018A>G VV NP_001166286.1:p.=
NM_173851.2:c.*1018A>G VV NP_776250.2:p.=
XM_011516881.1:c.*1018A>G XP_011515183.1:p.=
XM_011516882.1:c.*1018A>G XP_011515184.1:p.=
XR_928566.1:n.920-211T>C
XR_928567.1:n.513-211T>C
XR_928568.1:n.718-211T>C
XR_928569.1:n.761-211T>C
XR_928570.1:n.761-211T>C
NM_001172815.2:c.*1018A>G VV NP_001166286.1:p.=
XM_024447083.1:c.*1018A>G XP_024302851.1:p.=
XR_001746038.1:n.705-211T>C
XR_928566.2:n.863-211T>C
XR_928567.2:n.476-211T>C
XR_928568.3:n.716-211T>C
XR_928569.2:n.714-211T>C
XR_928570.2:n.714-211T>C
ENST00000427715.2:c.*1018A>G ENSP00000407505.2:p.=
ENST00000456015.6:n.2128A>G ENSP00000415011.2:p.=
ENST00000519688.5:c.*1018A>G ENSP00000431069.1:p.=