Canonical Allele Identifier: CA2695449174

Gene: SDHB

Linked Data

• dbSNP Id: rs2101514068

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022738_17022739insGAACTGCAGGCC , CM000663.2:g.17022738_17022739insGAACTGCAGGCC	GRCh38
NC_000001.10:g.17349233_17349234insGAACTGCAGGCC , CM000663.1:g.17349233_17349234insGAACTGCAGGCC	GRCh37
NC_000001.9:g.17221820_17221821insGAACTGCAGGCC	NCBI36
NG_012340.1:g.36432_36433insGGCCTGCAGTTC , LRG_316:g.36432_36433insGGCCTGCAGTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.472-9_472-8insGGCCTGCAGTTC	ENSP00000481376.2:n.472-9_472-8insGGCCTGCAGTTC
ENST00000491274.6:c.601-9_601-8insGGCCTGCAGTTC	ENSP00000480482.2:n.601-9_601-8insGGCCTGCAGTTC
ENST00000375499.8:c.643-9_643-8insGGCCTGCAGTTC MANE Select	ENSP00000364649.3:n.643-9_643-8insGGCCTGCAGTTC
ENST00000375499.7:c.643-9_643-8insGGCCTGCAGTTC	ENSP00000364649.3:n.643-9_643-8insGGCCTGCAGTTC
ENST00000475049.5:n.68-9_68-8insGGCCTGCAGTTC
ENST00000485092.5:n.298_299insGGCCTGCAGTTC
ENST00000485515.5:n.577-9_577-8insGGCCTGCAGTTC
NM_003000.2:c.643-9_643-8insGGCCTGCAGTTC , LRG_316t1:c.643-9_643-8insGGCCTGCAGTTC	NP_002991.2:n.643-9_643-8insGGCCTGCAGTTC
NM_003000.3:c.643-9_643-8insGGCCTGCAGTTC MANE Select	NP_002991.2:n.643-9_643-8insGGCCTGCAGTTC