Canonical Allele Identifier: CA2586964060
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027836_17027840del , CM000663.2:g.17027836_17027840del GRCh38
NC_000001.10:g.17354331_17354335del , CM000663.1:g.17354331_17354335del GRCh37
NC_000001.9:g.17226918_17226922del NCBI36
NG_012340.1:g.31331_31335del , LRG_316:g.31331_31335del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.278_282del ENSP00000481376.2:p.Tyr93PhefsTer3
ENST00000491274.6:c.407_411del ENSP00000480482.2:p.Tyr136PhefsTer3
ENST00000375499.8:c.449_453del MANE Select ENSP00000364649.3:p.Tyr150PhefsTer3
ENST00000375499.7:c.449_453del ENSP00000364649.3:p.Tyr150PhefsTer3
ENST00000463045.2:c.278_282del ENSP00000481376.1:p.Tyr93PhefsTer3
ENST00000475506.1:n.366_370del
ENST00000485515.5:n.383_387del
ENST00000491274.5:c.407_411del ENSP00000480482.1:p.Tyr136PhefsTer3
NM_003000.2:c.449_453del , LRG_316t1:c.449_453del NP_002991.2:p.Tyr150PhefsTer3
NM_003000.3:c.449_453del MANE Select NP_002991.2:p.Tyr150PhefsTer3