Canonical Allele Identifier: CA1156078582
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023919A= , CM000663.2:g.17023919A= GRCh38
NC_000001.10:g.17350414A= , CM000663.1:g.17350414A= GRCh37
NC_000001.9:g.17223001A= NCBI36
NG_012340.1:g.35252T= , LRG_316:g.35252T=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.471+54T= ENSP00000481376.2:n.471+54T=
ENST00000491274.6:c.600+54T= ENSP00000480482.2:n.600+54T=
ENST00000375499.8:c.642+54T= MANE Select ENSP00000364649.3:n.642+54T=
ENST00000375499.7:c.642+54T= ENSP00000364649.3:n.642+54T=
ENST00000485515.5:n.576+54T=
NM_003000.2:c.642+54T= , LRG_316t1:c.642+54T= NP_002991.2:n.642+54T=
NM_003000.3:c.642+54T= MANE Select NP_002991.2:n.642+54T=