Canonical Allele Identifier: CA1156077833
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022304_17022306delinsTTC , CM000663.2:g.17022304_17022306delinsTTC GRCh38
NC_000001.10:g.17348799_17348801delinsTTC , CM000663.1:g.17348799_17348801delinsTTC GRCh37
NC_000001.9:g.17221386_17221388delinsTTC NCBI36
NG_012340.1:g.36865_36867delinsGAA , LRG_316:g.36865_36867delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+302_594+304delinsGAA ENSP00000481376.2:n.594+302_594+304delinsGAA
ENST00000491274.6:c.723+302_723+304delinsGAA ENSP00000480482.2:n.723+302_723+304delinsGAA
ENST00000375499.8:c.765+302_765+304delinsGAA MANE Select ENSP00000364649.3:n.765+302_765+304delinsGAA
ENST00000375499.7:c.765+302_765+304delinsGAA ENSP00000364649.3:n.765+302_765+304delinsGAA
ENST00000475049.5:n.190+302_190+304delinsGAA
ENST00000485092.5:n.429+302_429+304delinsGAA
NM_003000.2:c.765+302_765+304delinsGAA , LRG_316t1:c.765+302_765+304delinsGAA NP_002991.2:n.765+302_765+304delinsGAA
NM_003000.3:c.765+302_765+304delinsGAA MANE Select NP_002991.2:n.765+302_765+304delinsGAA