Canonical Allele Identifier: CA1156077939
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022551T= , CM000663.2:g.17022551T= GRCh38
NC_000001.10:g.17349046T= , CM000663.1:g.17349046T= GRCh37
NC_000001.9:g.17221633T= NCBI36
NG_012340.1:g.36620A= , LRG_316:g.36620A=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+57A= ENSP00000481376.2:n.594+57A=
ENST00000491274.6:c.723+57A= ENSP00000480482.2:n.723+57A=
ENST00000375499.8:c.765+57A= MANE Select ENSP00000364649.3:n.765+57A=
ENST00000375499.7:c.765+57A= ENSP00000364649.3:n.765+57A=
ENST00000475049.5:n.190+57A=
ENST00000485092.5:n.429+57A=
NM_003000.2:c.765+57A= , LRG_316t1:c.765+57A= NP_002991.2:n.765+57A=
NM_003000.3:c.765+57A= MANE Select NP_002991.2:n.765+57A=