Canonical Allele Identifier: CA16609908

Gene: SDHC

Linked Data

• ClinVar Variation Id: 414249
• ClinVar RCV Id: RCV000473036
• dbSNP Id: rs1060504224
• gnomAD v2: 1-161284225-G-A
• gnomAD v4: 1-161314435-G-A
• MyVariant Identifiers: chr1:g.161284225G>A (hg19) ; chr1:g.161314435G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161314435G>A , CM000663.2:g.161314435G>A	GRCh38
NC_000001.10:g.161284225G>A , CM000663.1:g.161284225G>A	GRCh37
NC_000001.9:g.159550849G>A	NCBI36
NG_008055.1:g.538C>T , LRG_256:g.538C>T
NG_012767.1:g.5060G>A , LRG_317:g.5060G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.20+10G>A	ENSP00000482902.2:n.20+10G>A
ENST00000367975.7:c.20+10G>A MANE Select	ENSP00000356953.3:n.20+10G>A
ENST00000342751.8:c.20+10G>A	ENSP00000356952.3:n.20+10G>A
ENST00000367975.6:c.20+10G>A	ENSP00000356953.2:n.20+10G>A
ENST00000392169.6:c.20+10G>A	ENSP00000376009.2:n.20+10G>A
ENST00000432287.6:c.20+10G>A	ENSP00000390558.2:n.20+10G>A
ENST00000504963.5:c.20+10G>A	ENSP00000423929.1:n.20+10G>A
ENST00000513009.5:c.20+10G>A	ENSP00000423260.1:n.20+10G>A
ENST00000515731.1:n.55G>A
NM_001035511.1:c.20+10G>A	NP_001030588.1:n.20+10G>A
NM_001035512.1:c.20+10G>A	NP_001030589.1:n.20+10G>A
NM_001035513.1:c.20+10G>A	NP_001030590.1:n.20+10G>A
NM_001278172.1:c.20+10G>A	NP_001265101.1:n.20+10G>A
NM_003001.3:c.20+10G>A , LRG_317t1:c.20+10G>A	NP_002992.1:n.20+10G>A
NR_103459.1:n.50+10G>A
NM_001035511.2:c.20+10G>A	NP_001030588.1:n.20+10G>A
NM_001035512.2:c.20+10G>A	NP_001030589.1:n.20+10G>A
NM_001035513.2:c.20+10G>A	NP_001030590.1:n.20+10G>A
NM_001278172.2:c.20+10G>A	NP_001265101.1:n.20+10G>A
NM_003001.5:c.20+10G>A MANE Select	NP_002992.1:n.20+10G>A
NR_103459.2:n.45+10G>A