Canonical Allele Identifier: CA338272869

Gene: SDHB

Linked Data

• ClinVar Variation Id: 3073992
• ClinVar RCV Id: RCV004012534
• gnomAD v4: 1-17027813-T-C
• MyVariant Identifiers: chr1:g.17354308T>C (hg19) ; chr1:g.17027813T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027813T>C , CM000663.2:g.17027813T>C	GRCh38
NC_000001.10:g.17354308T>C , CM000663.1:g.17354308T>C	GRCh37
NC_000001.9:g.17226895T>C	NCBI36
NG_012340.1:g.31358A>G , LRG_316:g.31358A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.305A>G	ENSP00000481376.2:p.Lys102Arg
ENST00000491274.6:c.434A>G	ENSP00000480482.2:p.Lys145Arg
ENST00000375499.8:c.476A>G MANE Select	ENSP00000364649.3:p.Lys159Arg
ENST00000375499.7:c.476A>G	ENSP00000364649.3:p.Lys159Arg
ENST00000463045.2:c.305A>G	ENSP00000481376.1:p.Lys102Arg
ENST00000475506.1:n.393A>G
ENST00000485515.5:n.410A>G
ENST00000491274.5:c.434A>G	ENSP00000480482.1:p.Lys145Arg
NM_003000.2:c.476A>G , LRG_316t1:c.476A>G	NP_002991.2:p.Lys159Arg
NM_003000.3:c.476A>G MANE Select	NP_002991.2:p.Lys159Arg