Canonical Allele Identifier: CA1156078566
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023894T= , CM000663.2:g.17023894T= GRCh38
NC_000001.10:g.17350389T= , CM000663.1:g.17350389T= GRCh37
NC_000001.9:g.17222976T= NCBI36
NG_012340.1:g.35277A= , LRG_316:g.35277A=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.471+79A= ENSP00000481376.2:n.471+79A=
ENST00000491274.6:c.600+79A= ENSP00000480482.2:n.600+79A=
ENST00000375499.8:c.642+79A= MANE Select ENSP00000364649.3:n.642+79A=
ENST00000375499.7:c.642+79A= ENSP00000364649.3:n.642+79A=
ENST00000485515.5:n.576+79A=
NM_003000.2:c.642+79A= , LRG_316t1:c.642+79A= NP_002991.2:n.642+79A=
NM_003000.3:c.642+79A= MANE Select NP_002991.2:n.642+79A=