LDH info

Canonical Allele Identifier: CA8070077
Gene: SLC12A3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372504
ClinVar RCV Id: RCV000412851
dbSNP Id: rs199974259

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56902509G>T , CM000678.2:g.56902509G>T GRCh38
NC_000016.9:g.56936421G>T , CM000678.1:g.56936421G>T GRCh37
NC_000016.8:g.55493922G>T NCBI36
NG_009386.1:g.42303G>T
NG_009386.2:g.42303G>T

Transcript Alleles

HGVS Amino-acid change
NM_000339.2:c.2883+1G>T VV NP_000330.2:p.=
NM_001126107.1:c.2880+1G>T VV NP_001119579.1:p.=
NM_001126108.1:c.2856+1G>T VV NP_001119580.1:p.=
XM_005256119.1:c.2853+1G>T XP_005256176.1:p.=
XM_005256119.2:c.2853+1G>T XP_005256176.1:p.=
NM_000339.3:c.2883+1G>T VV NP_000330.3:p.=
NM_001126107.2:c.2880+1G>T VV NP_001119579.2:p.=
NM_001126108.2:c.2856+1G>T VV MANE Preferred NP_001119580.2:p.=
ENST00000262502.5:c.2853+1G>T ENSP00000262502.5:p.=
ENST00000438926.6:c.2883+1G>T ENSP00000402152.2:p.=
ENST00000563236.5:c.2856+1G>T ENSP00000456149.1:p.=
ENST00000566786.5:c.2880+1G>T ENSP00000457552.1:p.=
ENST00000569002.1:n.287+1G>T