Canonical Allele Identifier: CA1156080092
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027607G= , CM000663.2:g.17027607G= GRCh38
NC_000001.10:g.17354102G= , CM000663.1:g.17354102G= GRCh37
NC_000001.9:g.17226689G= NCBI36
NG_012340.1:g.31564C= , LRG_316:g.31564C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+142C= ENSP00000481376.2:n.369+142C=
ENST00000491274.6:c.498+142C= ENSP00000480482.2:n.498+142C=
ENST00000375499.8:c.540+142C= MANE Select ENSP00000364649.3:n.540+142C=
ENST00000375499.7:c.540+142C= ENSP00000364649.3:n.540+142C=
ENST00000485515.5:n.474+142C=
ENST00000491274.5:c.498+142C= ENSP00000480482.1:n.498+142C=
NM_003000.2:c.540+142C= , LRG_316t1:c.540+142C= NP_002991.2:n.540+142C=
NM_003000.3:c.540+142C= MANE Select NP_002991.2:n.540+142C=