Canonical Allele Identifier: CA338273039
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1570947938

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027827C>A , CM000663.2:g.17027827C>A GRCh38
NC_000001.10:g.17354322C>A , CM000663.1:g.17354322C>A GRCh37
NC_000001.9:g.17226909C>A NCBI36
NG_012340.1:g.31344G>T , LRG_316:g.31344G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.291G>T ENSP00000481376.2:p.Glu97Asp
ENST00000491274.6:c.420G>T ENSP00000480482.2:p.Glu140Asp
ENST00000375499.8:c.462G>T MANE Select ENSP00000364649.3:p.Glu154Asp
ENST00000375499.7:c.462G>T ENSP00000364649.3:p.Glu154Asp
ENST00000463045.2:c.291G>T ENSP00000481376.1:p.Glu97Asp
ENST00000475506.1:n.379G>T
ENST00000485515.5:n.396G>T
ENST00000491274.5:c.420G>T ENSP00000480482.1:p.Glu140Asp
NM_003000.2:c.462G>T , LRG_316t1:c.462G>T NP_002991.2:p.Glu154Asp
NM_003000.3:c.462G>T MANE Select NP_002991.2:p.Glu154Asp