Canonical Allele Identifier: CA1156080111
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027651T= , CM000663.2:g.17027651T= GRCh38
NC_000001.10:g.17354146T= , CM000663.1:g.17354146T= GRCh37
NC_000001.9:g.17226733T= NCBI36
NG_012340.1:g.31520A= , LRG_316:g.31520A=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+98A= ENSP00000481376.2:n.369+98A=
ENST00000491274.6:c.498+98A= ENSP00000480482.2:n.498+98A=
ENST00000375499.8:c.540+98A= MANE Select ENSP00000364649.3:n.540+98A=
ENST00000375499.7:c.540+98A= ENSP00000364649.3:n.540+98A=
ENST00000485515.5:n.474+98A=
ENST00000491274.5:c.498+98A= ENSP00000480482.1:n.498+98A=
NM_003000.2:c.540+98A= , LRG_316t1:c.540+98A= NP_002991.2:n.540+98A=
NM_003000.3:c.540+98A= MANE Select NP_002991.2:n.540+98A=