Canonical Allele Identifier: CA1156080200
Gene: SDHB HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.271G= ENSP00000481376.2:p.Ala91=
ENST00000491274.6:c.400G= ENSP00000480482.2:p.Ala134=
ENST00000375499.8:c.442G= MANE Select ENSP00000364649.3:p.Ala148=
ENST00000375499.7:c.442G= ENSP00000364649.3:p.Ala148=
ENST00000463045.2:c.271G= ENSP00000481376.1:p.Ala91=
ENST00000475506.1:n.359G=
ENST00000485515.5:n.376G=
ENST00000491274.5:c.400G= ENSP00000480482.1:p.Ala134=
NM_003000.2:c.442G= , LRG_316t1:c.442G= NP_002991.2:p.Ala148=
NM_003000.3:c.442G= MANE Select NP_002991.2:p.Ala148=