LDH info

Canonical Allele Identifier: CA129915230
Gene: SLC36A3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10061997

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151279426T>C , CM000667.2:g.151279426T>C GRCh38
NC_000005.9:g.150658987T>C , CM000667.1:g.150658987T>C GRCh37
NC_000005.8:g.150639180T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001145017.1:c.1267+1588A>G VV NP_001138489.1:p.=
NM_181774.3:c.1144+1588A>G VV NP_861439.3:p.=
XM_006714781.1:c.995-1765A>G XP_006714844.1:p.=
XM_011537626.1:c.1138+1588A>G XP_011535928.1:p.=
XM_011537627.1:c.1066+1588A>G XP_011535929.1:p.=
XM_011537628.1:c.1000+1588A>G XP_011535930.1:p.=
XM_011537629.1:c.975-1765A>G XP_011535931.1:p.=
XM_011537630.1:c.799+1588A>G XP_011535932.1:p.=
XM_011537631.1:c.799+1588A>G XP_011535933.1:p.=
XM_011537632.1:c.799+1588A>G XP_011535934.1:p.=
XM_011537633.1:c.655+1588A>G XP_011535935.1:p.=
XR_427775.1:n.1592+1588A>G
XM_011537627.3:c.1066+1588A>G XP_011535929.1:p.=
XM_011537629.3:c.975-1765A>G XP_011535931.1:p.=
XM_011537630.2:c.799+1588A>G XP_011535932.1:p.=
XM_011537631.2:c.799+1588A>G XP_011535933.1:p.=
XR_427775.3:n.1576+1588A>G
ENST00000335230.7:c.1144+1588A>G ENSP00000334750.3:p.=
ENST00000377713.3:c.1267+1588A>G ENSP00000366942.3:p.=
ENST00000423071.2:n.3044+1588A>G