Canonical Allele Identifier: CA31433693

Gene: SDHC

Linked Data

• ClinVar Variation Id: 2009177
• ClinVar RCV Id: RCV002838153
• dbSNP Id: rs369274171
• MyVariant Identifiers: chr1:g.161326643G>T (hg19) ; chr1:g.161356853G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161356853G>T , CM000663.2:g.161356853G>T	GRCh38
NC_000001.10:g.161326643G>T , CM000663.1:g.161326643G>T	GRCh37
NC_000001.9:g.159593267G>T	NCBI36
NG_012767.1:g.47478G>T , LRG_317:g.47478G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.*406+13G>T	ENSP00000482902.2:n.*406+13G>T
ENST00000367975.7:c.405+13G>T MANE Select	ENSP00000356953.3:n.405+13G>T
ENST00000342751.8:c.242-5476G>T	ENSP00000356952.3:n.242-5476G>T
ENST00000367975.6:c.405+13G>T	ENSP00000356953.2:n.405+13G>T
ENST00000392169.6:c.246+13G>T	ENSP00000376009.2:n.246+13G>T
ENST00000432287.6:c.303+13G>T	ENSP00000390558.2:n.303+13G>T
ENST00000470743.4:c.503+13G>T
ENST00000504963.5:c.*228+13G>T	ENSP00000423929.1:n.*228+13G>T
ENST00000513009.5:c.140-5476G>T	ENSP00000423260.1:n.140-5476G>T
NM_001035511.1:c.242-5476G>T	NP_001030588.1:n.242-5476G>T
NM_001035512.1:c.303+13G>T	NP_001030589.1:n.303+13G>T
NM_001035513.1:c.246+13G>T	NP_001030590.1:n.246+13G>T
NM_001278172.1:c.140-5476G>T	NP_001265101.1:n.140-5476G>T
NM_003001.3:c.405+13G>T , LRG_317t1:c.405+13G>T	NP_002992.1:n.405+13G>T
NR_103459.1:n.462+13G>T
NM_001035511.2:c.242-5476G>T	NP_001030588.1:n.242-5476G>T
NM_001035512.2:c.303+13G>T	NP_001030589.1:n.303+13G>T
NM_001035513.2:c.246+13G>T	NP_001030590.1:n.246+13G>T
NM_001278172.2:c.140-5476G>T	NP_001265101.1:n.140-5476G>T
NM_003001.5:c.405+13G>T MANE Select	NP_002992.1:n.405+13G>T
NR_103459.2:n.457+13G>T