LDH info

Canonical Allele Identifier: CA016759
Gene: SDHD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6892
dbSNP Id: rs104894303

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112087910C>T , CM000673.2:g.112087910C>T GRCh38
NC_000011.9:g.111958634C>T , CM000673.1:g.111958634C>T GRCh37
NC_000011.8:g.111463844C>T NCBI36
NG_012337.2:g.6064C>T
NG_033145.1:g.3889G>A
NG_012337.3:g.6064C>T

Transcript Alleles

HGVS Amino-acid change
NM_001276503.1:c.106C>T VV NP_001263432.1:p.Gln36Ter
NM_001276504.1:c.52+951C>T VV NP_001263433.1:p.=
NM_001276506.1:c.106C>T VV NP_001263435.1:p.Gln36Ter
NM_003002.3:c.106C>T VV NP_002993.1:p.Gln36Ter
NR_077060.1:n.190C>T
NM_003002.4:c.106C>T VV MANE Preferred NP_002993.1:p.Gln36Ter
NM_001276503.2:c.106C>T VV NP_001263432.1:p.Gln36Ter
NM_001276504.2:c.52+951C>T VV NP_001263433.1:p.=
NM_001276506.2:c.106C>T VV NP_001263435.1:p.Gln36Ter
NR_077060.2:n.141C>T
ENST00000375549.7:c.106C>T ENSP00000364699.3:p.Gln36Ter
ENST00000525291.5:c.52+951C>T ENSP00000436669.1:p.=
ENST00000525987.5:n.111C>T
ENST00000526592.5:c.106C>T ENSP00000432005.1:p.Gln36Ter
ENST00000528021.5:c.106C>T ENSP00000432465.1:p.Gln36Ter
ENST00000528048.5:c.106C>T ENSP00000436217.1:p.Gln36Ter
ENST00000528182.5:c.106C>T ENSP00000435475.1:p.Gln36Ter
ENST00000530923.5:n.96C>T
ENST00000531744.5:c.106C>T ENSP00000456957.1:p.Gln36Ter
ENST00000532699.1:c.106C>T ENSP00000456434.1:p.Gln36Ter
ENST00000614349.4:c.106C>T ENSP00000480666.1:p.Gln36Ter