Canonical Allele Identifier: CA1156077791
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077965434

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022190_17022191del , CM000663.2:g.17022190_17022191del GRCh38
NC_000001.10:g.17348685_17348686del , CM000663.1:g.17348685_17348686del GRCh37
NC_000001.9:g.17221272_17221273del NCBI36
NG_012340.1:g.36980_36981del , LRG_316:g.36980_36981del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+417_594+418del ENSP00000481376.2:n.594+417_594+418del
ENST00000491274.6:c.723+417_723+418del ENSP00000480482.2:n.723+417_723+418del
ENST00000375499.8:c.765+417_765+418del MANE Select ENSP00000364649.3:n.765+417_765+418del
ENST00000375499.7:c.765+417_765+418del ENSP00000364649.3:n.765+417_765+418del
ENST00000475049.5:n.190+417_190+418del
ENST00000485092.5:n.429+417_429+418del
NM_003000.2:c.765+417_765+418del , LRG_316t1:c.765+417_765+418del NP_002991.2:n.765+417_765+418del
NM_003000.3:c.765+417_765+418del MANE Select NP_002991.2:n.765+417_765+418del