LDH info

Canonical Allele Identifier: CA11741948
Gene: F11 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2036914

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186271327T>C , CM000666.2:g.186271327T>C GRCh38
NC_000004.11:g.187192481T>C , CM000666.1:g.187192481T>C GRCh37
NC_000004.10:g.187429475T>C NCBI36
NG_008051.1:g.10364T>C , LRG_583:g.10364T>C

Transcript Alleles

HGVS Amino-acid change
NM_000128.3:c.56-282T>C , LRG_583t1:c.56-282T>C NP_000119.1:p.=
XM_005262821.2:c.56-282T>C XP_005262878.1:p.=
XM_005262822.2:c.56-282T>C XP_005262879.1:p.=
XM_005262823.2:c.56-282T>C XP_005262880.1:p.=
XM_005262824.1:c.56-282T>C XP_005262881.1:p.=
XM_006714137.1:c.56-282T>C XP_006714200.1:p.=
XR_938706.1:n.408-282T>C
XR_938707.1:n.408-282T>C
NM_001354804.1:c.56-282T>C VV NP_001341733.1:p.=
XM_005262821.4:c.56-282T>C XP_005262878.1:p.=
XM_005262822.4:c.56-282T>C XP_005262879.1:p.=
XM_005262823.4:c.56-282T>C XP_005262880.1:p.=
XM_006714137.3:c.56-282T>C XP_006714200.1:p.=
XM_017007884.2:c.56-282T>C XP_016863373.1:p.=
XM_017007885.2:c.56-282T>C XP_016863374.1:p.=
XM_017007886.2:c.56-282T>C XP_016863375.1:p.=
XR_001741172.2:n.389-282T>C
NM_000128.4:c.56-282T>C VV MANE Preferred NP_000119.1:p.=
NM_001354804.2:c.56-282T>C VV NP_001341733.1:p.=
ENST00000264692.8:c.56-282T>C ENSP00000264692.5:p.=
ENST00000403665.6:c.56-282T>C ENSP00000384957.2:p.=
ENST00000492972.6:c.56-282T>C ENSP00000424479.1:p.=