Canonical Allele Identifier: CA1156080113
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027657G= , CM000663.2:g.17027657G= GRCh38
NC_000001.10:g.17354152G= , CM000663.1:g.17354152G= GRCh37
NC_000001.9:g.17226739G= NCBI36
NG_012340.1:g.31514C= , LRG_316:g.31514C=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+92C= ENSP00000481376.2:n.369+92C=
ENST00000491274.6:c.498+92C= ENSP00000480482.2:n.498+92C=
ENST00000375499.8:c.540+92C= MANE Select ENSP00000364649.3:n.540+92C=
ENST00000375499.7:c.540+92C= ENSP00000364649.3:n.540+92C=
ENST00000475506.1:n.549C=
ENST00000485515.5:n.474+92C=
ENST00000491274.5:c.498+92C= ENSP00000480482.1:n.498+92C=
NM_003000.2:c.540+92C= , LRG_316t1:c.540+92C= NP_002991.2:n.540+92C=
NM_003000.3:c.540+92C= MANE Select NP_002991.2:n.540+92C=