Canonical Allele Identifier: CA1156077976
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022629G= , CM000663.2:g.17022629G= GRCh38
NC_000001.10:g.17349124G= , CM000663.1:g.17349124G= GRCh37
NC_000001.9:g.17221711G= NCBI36
NG_012340.1:g.36542C= , LRG_316:g.36542C=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.573C= ENSP00000481376.2:p.Asn191=
ENST00000491274.6:c.702C= ENSP00000480482.2:p.Asn234=
ENST00000375499.8:c.744C= MANE Select ENSP00000364649.3:p.Asn248=
ENST00000375499.7:c.744C= ENSP00000364649.3:p.Asn248=
ENST00000475049.5:n.169C=
ENST00000485092.5:n.408C=
ENST00000485515.5:n.678C=
NM_003000.2:c.744C= , LRG_316t1:c.744C= NP_002991.2:p.Asn248=
NM_003000.3:c.744C= MANE Select NP_002991.2:p.Asn248=