Canonical Allele Identifier: CA1156078572
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077976771

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023904dup , CM000663.2:g.17023904dup GRCh38
NC_000001.10:g.17350399dup , CM000663.1:g.17350399dup GRCh37
NC_000001.9:g.17222986dup NCBI36
NG_012340.1:g.35267dup , LRG_316:g.35267dup

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.471+69dup ENSP00000481376.2:n.471+69dup
ENST00000491274.6:c.600+69dup ENSP00000480482.2:n.600+69dup
ENST00000375499.8:c.642+69dup MANE Select ENSP00000364649.3:n.642+69dup
ENST00000375499.7:c.642+69dup ENSP00000364649.3:n.642+69dup
ENST00000485515.5:n.576+69dup
NM_003000.2:c.642+69dup , LRG_316t1:c.642+69dup NP_002991.2:n.642+69dup
NM_003000.3:c.642+69dup MANE Select NP_002991.2:n.642+69dup