Canonical Allele Identifier: CA18665969
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs545307760

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027828T>C , CM000663.2:g.17027828T>C GRCh38
NC_000001.10:g.17354323T>C , CM000663.1:g.17354323T>C GRCh37
NC_000001.9:g.17226910T>C NCBI36
NG_012340.1:g.31343A>G , LRG_316:g.31343A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.290A>G ENSP00000481376.2:p.Glu97Gly
ENST00000491274.6:c.419A>G ENSP00000480482.2:p.Glu140Gly
ENST00000375499.8:c.461A>G MANE Select ENSP00000364649.3:p.Glu154Gly
ENST00000375499.7:c.461A>G ENSP00000364649.3:p.Glu154Gly
ENST00000463045.2:c.290A>G ENSP00000481376.1:p.Glu97Gly
ENST00000475506.1:n.378A>G
ENST00000485515.5:n.395A>G
ENST00000491274.5:c.419A>G ENSP00000480482.1:p.Glu140Gly
NM_003000.2:c.461A>G , LRG_316t1:c.461A>G NP_002991.2:p.Glu154Gly
NM_003000.3:c.461A>G MANE Select NP_002991.2:p.Glu154Gly