LDH info

Canonical Allele Identifier: CA212929

Identifiers and link-outs to other resources

ClinVar Variation Id: 11890
ClinVar RCV Id: RCV000012665
dbSNP Id: rs373297713

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186287824G>A , CM000666.2:g.186287824G>A GRCh38
NC_000004.11:g.187208978G>A , CM000666.1:g.187208978G>A GRCh37
NC_000004.10:g.187445972G>A NCBI36
NG_008051.1:g.26861G>A , LRG_583:g.26861G>A

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.1716+1G>A , LRG_583t1:c.1716+1G>A (F11) NP_000119.1:p.=
NR_033900.1:n.1066+604C>T (F11-AS1)
XM_005262821.2:c.1719+1G>A (F11) XP_005262878.1:p.=
XM_005262822.2:c.1623+1G>A (F11) XP_005262879.1:p.=
XM_005262823.2:c.1449+1G>A (F11) XP_005262880.1:p.=
XM_006714137.1:c.1671+1G>A (F11) XP_006714200.1:p.=
XM_005262821.4:c.1719+1G>A (F11) XP_005262878.1:p.=
XM_005262822.4:c.1623+1G>A (F11) XP_005262879.1:p.=
XM_005262823.4:c.1449+1G>A (F11) XP_005262880.1:p.=
XM_006714137.3:c.1671+1G>A (F11) XP_006714200.1:p.=
NM_000128.4:c.1716+1G>A (F11) VV NP_000119.1:p.=
ENST00000264691.4:n.316+1G>A
ENST00000264692.8:c.1554+1G>A ENSP00000264692.5:p.=
ENST00000403665.6:c.1716+1G>A ENSP00000384957.2:p.=
ENST00000503841.1:n.235+1G>A