Canonical Allele Identifier: CA1156080099
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027616_17027617delinsAC , CM000663.2:g.17027616_17027617delinsAC GRCh38
NC_000001.10:g.17354111_17354112delinsAC , CM000663.1:g.17354111_17354112delinsAC GRCh37
NC_000001.9:g.17226698_17226699delinsAC NCBI36
NG_012340.1:g.31554_31555delinsGT , LRG_316:g.31554_31555delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+132_369+133delinsGT ENSP00000481376.2:n.369+132_369+133delinsGT
ENST00000491274.6:c.498+132_498+133delinsGT ENSP00000480482.2:n.498+132_498+133delinsGT
ENST00000375499.8:c.540+132_540+133delinsGT MANE Select ENSP00000364649.3:n.540+132_540+133delinsGT
ENST00000375499.7:c.540+132_540+133delinsGT ENSP00000364649.3:n.540+132_540+133delinsGT
ENST00000485515.5:n.474+132_474+133delinsGT
ENST00000491274.5:c.498+132_498+133delinsGT ENSP00000480482.1:n.498+132_498+133delinsGT
NM_003000.2:c.540+132_540+133delinsGT , LRG_316t1:c.540+132_540+133delinsGT NP_002991.2:n.540+132_540+133delinsGT
NM_003000.3:c.540+132_540+133delinsGT MANE Select NP_002991.2:n.540+132_540+133delinsGT