Canonical Allele Identifier: CA1156080142
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027731T= , CM000663.2:g.17027731T= GRCh38
NC_000001.10:g.17354226T= , CM000663.1:g.17354226T= GRCh37
NC_000001.9:g.17226813T= NCBI36
NG_012340.1:g.31440A= , LRG_316:g.31440A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+18A= ENSP00000481376.2:n.369+18A=
ENST00000491274.6:c.498+18A= ENSP00000480482.2:n.498+18A=
ENST00000375499.8:c.540+18A= MANE Select ENSP00000364649.3:n.540+18A=
ENST00000375499.7:c.540+18A= ENSP00000364649.3:n.540+18A=
ENST00000475506.1:n.475A=
ENST00000485515.5:n.474+18A=
ENST00000491274.5:c.498+18A= ENSP00000480482.1:n.498+18A=
NM_003000.2:c.540+18A= , LRG_316t1:c.540+18A= NP_002991.2:n.540+18A=
NM_003000.3:c.540+18A= MANE Select NP_002991.2:n.540+18A=