Canonical Allele Identifier: CA1156080168
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027784G= , CM000663.2:g.17027784G= GRCh38
NC_000001.10:g.17354279G= , CM000663.1:g.17354279G= GRCh37
NC_000001.9:g.17226866G= NCBI36
NG_012340.1:g.31387C= , LRG_316:g.31387C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.334C= ENSP00000481376.2:p.Gln112=
ENST00000491274.6:c.463C= ENSP00000480482.2:p.Gln155=
ENST00000375499.8:c.505C= MANE Select ENSP00000364649.3:p.Gln169=
ENST00000375499.7:c.505C= ENSP00000364649.3:p.Gln169=
ENST00000463045.2:c.334C= ENSP00000481376.1:p.Gln112=
ENST00000475506.1:n.422C=
ENST00000485515.5:n.439C=
ENST00000491274.5:c.463C= ENSP00000480482.1:p.Gln155=
NM_003000.2:c.505C= , LRG_316t1:c.505C= NP_002991.2:p.Gln169=
NM_003000.3:c.505C= MANE Select NP_002991.2:p.Gln169=