Canonical Allele Identifier: CA338228458

Gene: SDHB

Linked Data

• ClinVar Variation Id: 428925
• ClinVar RCV Id: RCV000492329 ; RCV001591132 ; RCV001059539
• dbSNP Id: rs1131691055
• MyVariant Identifiers: chr1:g.17371384C>T (hg19) ; chr1:g.17044889C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044889C>T , CM000663.2:g.17044889C>T	GRCh38
NC_000001.10:g.17371384C>T , CM000663.1:g.17371384C>T	GRCh37
NC_000001.9:g.17243971C>T	NCBI36
NG_012340.1:g.14282G>A , LRG_316:g.14282G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-99-1G>A	ENSP00000481376.2:n.-99-1G>A
ENST00000491274.6:c.31-1G>A	ENSP00000480482.2:n.31-1G>A
ENST00000375499.8:c.73-1G>A MANE Select	ENSP00000364649.3:n.73-1G>A
ENST00000375499.7:c.73-1G>A	ENSP00000364649.3:n.73-1G>A
ENST00000463045.2:c.-99-1G>A	ENSP00000481376.1:n.-99-1G>A
ENST00000466613.2:n.85-1G>A
ENST00000485515.5:n.61-1G>A
ENST00000491274.5:c.31-1G>A	ENSP00000480482.1:n.31-1G>A
NM_003000.2:c.73-1G>A , LRG_316t1:c.73-1G>A	NP_002991.2:n.73-1G>A
NM_003000.3:c.73-1G>A MANE Select	NP_002991.2:n.73-1G>A