Canonical Allele Identifier: CA1156077928
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022528C= , CM000663.2:g.17022528C= GRCh38
NC_000001.10:g.17349023C= , CM000663.1:g.17349023C= GRCh37
NC_000001.9:g.17221610C= NCBI36
NG_012340.1:g.36643G= , LRG_316:g.36643G=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+80G= ENSP00000481376.2:n.594+80G=
ENST00000491274.6:c.723+80G= ENSP00000480482.2:n.723+80G=
ENST00000375499.8:c.765+80G= MANE Select ENSP00000364649.3:n.765+80G=
ENST00000375499.7:c.765+80G= ENSP00000364649.3:n.765+80G=
ENST00000475049.5:n.190+80G=
ENST00000485092.5:n.429+80G=
NM_003000.2:c.765+80G= , LRG_316t1:c.765+80G= NP_002991.2:n.765+80G=
NM_003000.3:c.765+80G= MANE Select NP_002991.2:n.765+80G=