LDH info

Canonical Allele Identifier: CA14098981
Gene: IVD HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10518693

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40407823C>T , CM000677.2:g.40407823C>T GRCh38
NC_000015.9:g.40700022C>T , CM000677.1:g.40700022C>T GRCh37
NC_000015.8:g.38487314C>T NCBI36
NG_011986.1:g.7337C>T
NG_011986.2:g.7339C>T

Transcript Alleles

HGVS Amino-acid change
NM_001159508.1:c.154-116C>T VV NP_001152980.1:p.=
NM_002225.3:c.243+98C>T VV NP_002216.2:p.=
XM_005254350.2:n.243+98C>T XP_005254407.1:p.=
XM_005254356.2:n.243+98C>T XP_005254413.1:p.=
XM_006720491.2:c.186+98C>T XP_006720554.1:p.=
XM_006720492.2:n.243+98C>T XP_006720555.1:p.=
XM_006720493.2:n.243+98C>T XP_006720556.1:p.=
XM_006720494.2:n.243+98C>T XP_006720557.1:p.=
XM_006720495.2:n.243+98C>T XP_006720558.1:p.=
XM_011521523.1:n.243+98C>T XP_011519825.1:p.=
XM_011521524.1:n.243+98C>T XP_011519826.1:p.=
XR_243097.3:n.243+98C>T
XR_243098.2:n.243+98C>T
XR_429453.2:n.344+98C>T
NM_001159508.2:c.145-116C>T VV NP_001152980.2:p.=
NM_001354597.2:c.186+98C>T VV NP_001341526.1:p.=
NM_001354598.2:c.234+98C>T VV NP_001341527.2:p.=
NM_001354599.2:c.321+11C>T VV NP_001341528.2:p.=
NM_001354600.2:c.321+11C>T VV NP_001341529.2:p.=
NM_001354601.2:c.234+98C>T VV NP_001341530.2:p.=
NM_002225.4:c.234+98C>T VV NP_002216.3:p.=
NR_148925.1:n.644+98C>T
XM_006720495.3:c.243+98C>T XP_006720558.1:p.=
XM_017022149.1:c.330+11C>T XP_016877638.1:p.=
XM_017022150.1:c.330+11C>T XP_016877639.1:p.=
XM_017022153.1:c.330+11C>T XP_016877642.1:p.=
XM_017022154.2:c.273+11C>T XP_016877643.1:p.=
XM_017022155.2:c.330+11C>T XP_016877644.1:p.=
XM_017022157.1:c.330+11C>T XP_016877646.1:p.=
XM_017022158.2:c.330+11C>T XP_016877647.1:p.=
XR_001751263.1:n.593+98C>T
XR_001751264.1:n.634+98C>T
ENST00000479013.6:c.154-116C>T ENSP00000417990.2:p.=
ENST00000487418.6:c.243+98C>T ENSP00000418397.2:p.=
ENST00000558610.5:c.186+98C>T ENSP00000453821.1:p.=
ENST00000610693.4:c.330+11C>T ENSP00000479359.1:p.=