Canonical Allele Identifier: CA1156077844
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022329_17022330delinsCA , CM000663.2:g.17022329_17022330delinsCA GRCh38
NC_000001.10:g.17348824_17348825delinsCA , CM000663.1:g.17348824_17348825delinsCA GRCh37
NC_000001.9:g.17221411_17221412delinsCA NCBI36
NG_012340.1:g.36841_36842delinsTG , LRG_316:g.36841_36842delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+278_594+279delinsTG ENSP00000481376.2:n.594+278_594+279delinsTG
ENST00000491274.6:c.723+278_723+279delinsTG ENSP00000480482.2:n.723+278_723+279delinsTG
ENST00000375499.8:c.765+278_765+279delinsTG MANE Select ENSP00000364649.3:n.765+278_765+279delinsTG
ENST00000375499.7:c.765+278_765+279delinsTG ENSP00000364649.3:n.765+278_765+279delinsTG
ENST00000475049.5:n.190+278_190+279delinsTG
ENST00000485092.5:n.429+278_429+279delinsTG
NM_003000.2:c.765+278_765+279delinsTG , LRG_316t1:c.765+278_765+279delinsTG NP_002991.2:n.765+278_765+279delinsTG
NM_003000.3:c.765+278_765+279delinsTG MANE Select NP_002991.2:n.765+278_765+279delinsTG