Canonical Allele Identifier: CA089457

Gene: SDHC

Linked Data

• ClinVar Variation Id: 368837
• ClinVar RCV Id: RCV000287178 ; RCV000325790 ; RCV000290768 ; RCV000382819 ; RCV000406625 ; RCV000662850 ; RCV001101380 ; RCV001000114 ; RCV001653768 ; RCV001523188 ; RCV002256223 ; RCV002488835
• dbSNP Id: rs112556972
• ExAC: 1:161284158 G / A
• gnomAD v2: 1-161284158-G-A
• gnomAD v3: 1-161314368-G-A
• gnomAD v4: 1-161314368-G-A
• MyVariant Identifiers: chr1:g.161284158G>A (hg19) ; chr1:g.161314368G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161314368G>A , CM000663.2:g.161314368G>A	GRCh38
NC_000001.10:g.161284158G>A , CM000663.1:g.161284158G>A	GRCh37
NC_000001.9:g.159550782G>A	NCBI36
NG_008055.1:g.605C>T , LRG_256:g.605C>T
NG_012767.1:g.4993G>A , LRG_317:g.4993G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367975.6:c.-38G>A	ENSP00000356953.2:n.-38G>A