Canonical Allele Identifier: CA1156080393

Gene: SDHB

Linked Data

• dbSNP Id: rs2078002837

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028316_17028318del , CM000663.2:g.17028316_17028318del	GRCh38
NC_000001.10:g.17354811_17354813del , CM000663.1:g.17354811_17354813del	GRCh37
NC_000001.9:g.17227398_17227400del	NCBI36
NG_012340.1:g.30854_30856del , LRG_316:g.30854_30856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+283_252+285del	ENSP00000481376.2:n.252+283_252+285del
ENST00000491274.6:c.381+283_381+285del	ENSP00000480482.2:n.381+283_381+285del
ENST00000375499.8:c.423+283_423+285del MANE Select	ENSP00000364649.3:n.423+283_423+285del
ENST00000375499.7:c.423+283_423+285del	ENSP00000364649.3:n.423+283_423+285del
ENST00000463045.2:c.252+283_252+285del	ENSP00000481376.1:n.252+283_252+285del
ENST00000475506.1:n.340+283_340+285del
ENST00000485515.5:n.357+337_357+339del
ENST00000491274.5:c.381+283_381+285del	ENSP00000480482.1:n.381+283_381+285del
NM_003000.2:c.423+283_423+285del , LRG_316t1:c.423+283_423+285del	NP_002991.2:n.423+283_423+285del
NM_003000.3:c.423+283_423+285del MANE Select	NP_002991.2:n.423+283_423+285del