Canonical Allele Identifier: CA18661834
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs910785045

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022260_17022262del , CM000663.2:g.17022260_17022262del GRCh38
NC_000001.10:g.17348755_17348757del , CM000663.1:g.17348755_17348757del GRCh37
NC_000001.9:g.17221342_17221344del NCBI36
NG_012340.1:g.36913_36915del , LRG_316:g.36913_36915del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+350_594+352del ENSP00000481376.2:n.594+350_594+352del
ENST00000491274.6:c.723+350_723+352del ENSP00000480482.2:n.723+350_723+352del
ENST00000375499.8:c.765+350_765+352del MANE Select ENSP00000364649.3:n.765+350_765+352del
ENST00000375499.7:c.765+350_765+352del ENSP00000364649.3:n.765+350_765+352del
ENST00000475049.5:n.190+350_190+352del
ENST00000485092.5:n.429+350_429+352del
NM_003000.2:c.765+350_765+352del , LRG_316t1:c.765+350_765+352del NP_002991.2:n.765+350_765+352del
NM_003000.3:c.765+350_765+352del MANE Select NP_002991.2:n.765+350_765+352del