Canonical Allele Identifier: CA2574235828

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027902-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027902_17027903insG , CM000663.2:g.17027902_17027903insG	GRCh38
NC_000001.10:g.17354397_17354398insG , CM000663.1:g.17354397_17354398insG	GRCh37
NC_000001.9:g.17226984_17226985insG	NCBI36
NG_012340.1:g.31268_31269insC , LRG_316:g.31268_31269insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.253-38_253-37insC	ENSP00000481376.2:n.253-38_253-37insC
ENST00000491274.6:c.382-38_382-37insC	ENSP00000480482.2:n.382-38_382-37insC
ENST00000375499.8:c.424-38_424-37insC MANE Select	ENSP00000364649.3:n.424-38_424-37insC
ENST00000375499.7:c.424-38_424-37insC	ENSP00000364649.3:n.424-38_424-37insC
ENST00000463045.2:c.253-38_253-37insC	ENSP00000481376.1:n.253-38_253-37insC
ENST00000475506.1:n.341-38_341-37insC
ENST00000485515.5:n.358-38_358-37insC
ENST00000491274.5:c.382-38_382-37insC	ENSP00000480482.1:n.382-38_382-37insC
NM_003000.2:c.424-38_424-37insC , LRG_316t1:c.424-38_424-37insC	NP_002991.2:n.424-38_424-37insC
NM_003000.3:c.424-38_424-37insC MANE Select	NP_002991.2:n.424-38_424-37insC