Canonical Allele Identifier: CA338273198
Gene: SDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027840T>A , CM000663.2:g.17027840T>A GRCh38
NC_000001.10:g.17354335T>A , CM000663.1:g.17354335T>A GRCh37
NC_000001.9:g.17226922T>A NCBI36
NG_012340.1:g.31331A>T , LRG_316:g.31331A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.278A>T ENSP00000481376.2:p.Tyr93Phe
ENST00000491274.6:c.407A>T ENSP00000480482.2:p.Tyr136Phe
ENST00000375499.8:c.449A>T MANE Select ENSP00000364649.3:p.Tyr150Phe
ENST00000375499.7:c.449A>T ENSP00000364649.3:p.Tyr150Phe
ENST00000463045.2:c.278A>T ENSP00000481376.1:p.Tyr93Phe
ENST00000475506.1:n.366A>T
ENST00000485515.5:n.383A>T
ENST00000491274.5:c.407A>T ENSP00000480482.1:p.Tyr136Phe
NM_003000.2:c.449A>T , LRG_316t1:c.449A>T NP_002991.2:p.Tyr150Phe
NM_003000.3:c.449A>T MANE Select NP_002991.2:p.Tyr150Phe