Canonical Allele Identifier: CA416085864

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1109937
• ClinVar RCV Id: RCV001436012
• dbSNP Id: rs2101521627
• MyVariant Identifiers: chr1:g.17354277C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027782C>T , CM000663.2:g.17027782C>T	GRCh38
NC_000001.10:g.17354277C>T , CM000663.1:g.17354277C>T	GRCh37
NC_000001.9:g.17226864C>T	NCBI36
NG_012340.1:g.31389G>A , LRG_316:g.31389G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.336G>A	ENSP00000481376.2:p.Gln112=
ENST00000491274.6:c.465G>A	ENSP00000480482.2:p.Gln155=
ENST00000375499.8:c.507G>A MANE Select	ENSP00000364649.3:p.Gln169=
ENST00000375499.7:c.507G>A	ENSP00000364649.3:p.Gln169=
ENST00000463045.2:c.336G>A	ENSP00000481376.1:p.Gln112=
ENST00000475506.1:n.424G>A
ENST00000485515.5:n.441G>A
ENST00000491274.5:c.465G>A	ENSP00000480482.1:p.Gln155=
NM_003000.2:c.507G>A , LRG_316t1:c.507G>A	NP_002991.2:p.Gln169=
NM_003000.3:c.507G>A MANE Select	NP_002991.2:p.Gln169=