Canonical Allele Identifier: CA1148269913
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044917_17044925delinsAAAAAAAAA , CM000663.2:g.17044917_17044925delinsAAAAAAAAA GRCh38
NC_000001.10:g.17371412_17371420delinsAAAAAAAAA , CM000663.1:g.17371412_17371420delinsAAAAAAAAA GRCh37
NC_000001.9:g.17243999_17244007delinsAAAAAAAAA NCBI36
NG_012340.1:g.14246_14254delinsTTTTTTTTT , LRG_316:g.14246_14254delinsTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-99-37_-99-29delinsTTTTTTTTT ENSP00000481376.2:n.-99-37_-99-29delinsTTTTTTTTT
ENST00000491274.6:c.31-37_31-29delinsTTTTTTTTT ENSP00000480482.2:n.31-37_31-29delinsTTTTTTTTT
ENST00000375499.8:c.73-37_73-29delinsTTTTTTTTT MANE Select ENSP00000364649.3:n.73-37_73-29delinsTTTTTTTTT
ENST00000375499.7:c.73-37_73-29delinsTTTTTTTTT ENSP00000364649.3:n.73-37_73-29delinsTTTTTTTTT
ENST00000463045.2:c.-99-37_-99-29delinsTTTTTTTTT ENSP00000481376.1:n.-99-37_-99-29delinsTTTTTTTTT
ENST00000466613.2:n.85-37_85-29delinsTTTTTTTTT
ENST00000485515.5:n.61-37_61-29delinsTTTTTTTTT
ENST00000491274.5:c.31-37_31-29delinsTTTTTTTTT ENSP00000480482.1:n.31-37_31-29delinsTTTTTTTTT
NM_003000.2:c.73-37_73-29delinsTTTTTTTTT , LRG_316t1:c.73-37_73-29delinsTTTTTTTTT NP_002991.2:n.73-37_73-29delinsTTTTTTTTT
NM_003000.3:c.73-37_73-29delinsTTTTTTTTT MANE Select NP_002991.2:n.73-37_73-29delinsTTTTTTTTT