Canonical Allele Identifier: CA1139770655

Gene: SDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027880_17027881insGAA , CM000663.2:g.17027880_17027881insGAA	GRCh38
NC_000001.10:g.17354375_17354376insGAA , CM000663.1:g.17354375_17354376insGAA	GRCh37
NC_000001.9:g.17226962_17226963insGAA	NCBI36
NG_012340.1:g.31291_31292insTCT , LRG_316:g.31291_31292insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-15_253-14insTCT	ENSP00000481376.2:n.253-15_253-14insTCT
ENST00000491274.6:c.382-15_382-14insTCT	ENSP00000480482.2:n.382-15_382-14insTCT
ENST00000375499.8:c.424-15_424-14insTCT MANE Select	ENSP00000364649.3:n.424-15_424-14insTCT
ENST00000375499.7:c.424-15_424-14insTCT	ENSP00000364649.3:n.424-15_424-14insTCT
ENST00000463045.2:c.253-15_253-14insTCT	ENSP00000481376.1:n.253-15_253-14insTCT
ENST00000475506.1:n.341-15_341-14insTCT
ENST00000485515.5:n.358-15_358-14insTCT
ENST00000491274.5:c.382-15_382-14insTCT	ENSP00000480482.1:n.382-15_382-14insTCT
NM_003000.2:c.424-15_424-14insTCT , LRG_316t1:c.424-15_424-14insTCT	NP_002991.2:n.424-15_424-14insTCT
NM_003000.3:c.424-15_424-14insTCT MANE Select	NP_002991.2:n.424-15_424-14insTCT