Canonical Allele Identifier: CA1156078532
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077976444

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023832_17023841del , CM000663.2:g.17023832_17023841del GRCh38
NC_000001.10:g.17350327_17350336del , CM000663.1:g.17350327_17350336del GRCh37
NC_000001.9:g.17222914_17222923del NCBI36
NG_012340.1:g.35330_35339del , LRG_316:g.35330_35339del

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.471+132_471+141del ENSP00000481376.2:n.471+132_471+141del
ENST00000491274.6:c.600+132_600+141del ENSP00000480482.2:n.600+132_600+141del
ENST00000375499.8:c.642+132_642+141del MANE Select ENSP00000364649.3:n.642+132_642+141del
ENST00000375499.7:c.642+132_642+141del ENSP00000364649.3:n.642+132_642+141del
ENST00000485515.5:n.576+132_576+141del
NM_003000.2:c.642+132_642+141del , LRG_316t1:c.642+132_642+141del NP_002991.2:n.642+132_642+141del
NM_003000.3:c.642+132_642+141del MANE Select NP_002991.2:n.642+132_642+141del