LDH info

Canonical Allele Identifier: CA12737100
Gene: SLC30A8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4876703

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117151133C>A , CM000670.2:g.117151133C>A GRCh38
NC_000008.10:g.118163372C>A , CM000670.1:g.118163372C>A GRCh37
NC_000008.9:g.118232553C>A NCBI36
NG_016991.1:g.205861C>A

Transcript Alleles

HGVS Amino-acid change
NM_001172811.1:c.125-1811C>A VV NP_001166282.1:p.=
NM_001172813.1:c.125-1811C>A VV NP_001166284.1:p.=
NM_001172814.1:c.125-1811C>A VV NP_001166285.1:p.=
NM_001172815.1:c.125-1811C>A VV NP_001166286.1:p.=
NM_173851.2:c.272-1811C>A VV NP_776250.2:p.=
XM_011516881.1:c.272-1811C>A XP_011515183.1:p.=
XM_011516882.1:c.125-1811C>A XP_011515184.1:p.=
XR_928569.1:n.1020+21482G>T
XR_928570.1:n.1020+21482G>T
NM_001172815.2:c.125-1811C>A VV NP_001166286.1:p.=
XM_024447083.1:c.125-1811C>A XP_024302851.1:p.=
XR_928569.2:n.973+21482G>T
XR_928570.2:n.973+21482G>T
ENST00000427715.2:c.125-1811C>A ENSP00000407505.2:p.=
ENST00000456015.6:n.272-1811C>A ENSP00000415011.2:p.=
ENST00000518521.5:c.125-1811C>A ENSP00000485566.1:p.=
ENST00000519688.5:c.125-1811C>A ENSP00000431069.1:p.=
ENST00000521243.5:c.125-1811C>A ENSP00000428545.1:p.=
ENST00000524274.5:c.125-1811C>A ENSP00000427760.1:p.=