LDH info

Canonical Allele Identifier: CA16042288
Gene: SDHC HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372501
dbSNP Id: rs1057517818

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161328498G>C , CM000663.2:g.161328498G>C GRCh38
NC_000001.10:g.161298288G>C , CM000663.1:g.161298288G>C GRCh37
NC_000001.9:g.159564912G>C NCBI36
NG_012767.1:g.19123G>C , LRG_317:g.19123G>C

Transcript Alleles

HGVS Amino-acid change
NM_001035511.1:c.179+1G>C VV NP_001030588.1:p.=
NM_001035512.1:c.77+4828G>C VV NP_001030589.1:p.=
NM_001035513.1:c.21-12096G>C VV NP_001030590.1:p.=
NM_001278172.1:c.77+4828G>C VV NP_001265101.1:p.=
NM_003001.3:c.179+1G>C , LRG_317t1:c.179+1G>C NP_002992.1:p.=
NR_103459.1:n.209+1G>C
NM_001035511.2:c.179+1G>C VV NP_001030588.1:p.=
NM_001035512.2:c.77+4828G>C VV NP_001030589.1:p.=
NM_001035513.2:c.21-12096G>C VV NP_001030590.1:p.=
NM_001278172.2:c.77+4828G>C VV NP_001265101.1:p.=
NM_003001.5:c.179+1G>C VV MANE Preferred NP_002992.1:p.=
NR_103459.2:n.204+1G>C
ENST00000342751.8:c.179+1G>C ENSP00000356952.3:p.=
ENST00000367975.6:c.179+1G>C ENSP00000356953.2:p.=
ENST00000392169.6:c.21-12096G>C ENSP00000376009.2:p.=
ENST00000432287.6:c.77+4828G>C ENSP00000390558.2:p.=
ENST00000470743.4:n.277+1G>C
ENST00000504963.5:c.179+1G>C ENSP00000423929.1:p.=
ENST00000513009.5:c.77+4828G>C ENSP00000423260.1:p.=