Canonical Allele Identifier: CA338273338
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 999196
dbSNP Id: rs2078000133

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027847C>T , CM000663.2:g.17027847C>T GRCh38
NC_000001.10:g.17354342C>T , CM000663.1:g.17354342C>T GRCh37
NC_000001.9:g.17226929C>T NCBI36
NG_012340.1:g.31324G>A , LRG_316:g.31324G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.271G>A ENSP00000481376.2:p.Ala91Thr
ENST00000491274.6:c.400G>A ENSP00000480482.2:p.Ala134Thr
ENST00000375499.8:c.442G>A MANE Select ENSP00000364649.3:p.Ala148Thr
ENST00000375499.7:c.442G>A ENSP00000364649.3:p.Ala148Thr
ENST00000463045.2:c.271G>A ENSP00000481376.1:p.Ala91Thr
ENST00000475506.1:n.359G>A
ENST00000485515.5:n.376G>A
ENST00000491274.5:c.400G>A ENSP00000480482.1:p.Ala134Thr
NM_003000.2:c.442G>A , LRG_316t1:c.442G>A NP_002991.2:p.Ala148Thr
NM_003000.3:c.442G>A MANE Select NP_002991.2:p.Ala148Thr