Canonical Allele Identifier: CA2648776184

Gene: SDHC

Linked Data

• ClinVar Variation Id: 2934577
• ClinVar RCV Id: RCV003798279
• gnomAD v4: 1-161340659-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340659T>C , CM000663.2:g.161340659T>C	GRCh38
NC_000001.10:g.161310449T>C , CM000663.1:g.161310449T>C	GRCh37
NC_000001.9:g.159577073T>C	NCBI36
NG_012767.1:g.31284T>C , LRG_317:g.31284T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*242+4T>C	ENSP00000482902.2:n.*242+4T>C
ENST00000367975.7:c.241+4T>C MANE Select	ENSP00000356953.3:n.241+4T>C
ENST00000342751.8:c.241+4T>C	ENSP00000356952.3:n.241+4T>C
ENST00000367975.6:c.241+4T>C	ENSP00000356953.2:n.241+4T>C
ENST00000392169.6:c.82+4T>C	ENSP00000376009.2:n.82+4T>C
ENST00000432287.6:c.139+4T>C	ENSP00000390558.2:n.139+4T>C
ENST00000470743.4:c.339+4T>C
ENST00000504963.5:c.*64+4T>C	ENSP00000423929.1:n.*64+4T>C
ENST00000513009.5:c.139+4T>C	ENSP00000423260.1:n.139+4T>C
NM_001035511.1:c.241+4T>C	NP_001030588.1:n.241+4T>C
NM_001035512.1:c.139+4T>C	NP_001030589.1:n.139+4T>C
NM_001035513.1:c.82+4T>C	NP_001030590.1:n.82+4T>C
NM_001278172.1:c.139+4T>C	NP_001265101.1:n.139+4T>C
NM_003001.3:c.241+4T>C , LRG_317t1:c.241+4T>C	NP_002992.1:n.241+4T>C
NR_103459.1:n.298+4T>C
NM_001035511.2:c.241+4T>C	NP_001030588.1:n.241+4T>C
NM_001035512.2:c.139+4T>C	NP_001030589.1:n.139+4T>C
NM_001035513.2:c.82+4T>C	NP_001030590.1:n.82+4T>C
NM_001278172.2:c.139+4T>C	NP_001265101.1:n.139+4T>C
NM_003001.5:c.241+4T>C MANE Select	NP_002992.1:n.241+4T>C
NR_103459.2:n.293+4T>C