Canonical Allele Identifier: CA338276587
Gene: SDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17033117T>A , CM000663.2:g.17033117T>A GRCh38
NC_000001.10:g.17359612T>A , CM000663.1:g.17359612T>A GRCh37
NC_000001.9:g.17232199T>A NCBI36
NG_012340.1:g.26054A>T , LRG_316:g.26054A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.58A>T ENSP00000481376.2:p.Ile20Phe
ENST00000491274.6:c.187A>T ENSP00000480482.2:p.Ile63Phe
ENST00000375499.8:c.229A>T MANE Select ENSP00000364649.3:p.Ile77Phe
ENST00000375499.7:c.229A>T ENSP00000364649.3:p.Ile77Phe
ENST00000463045.2:c.58A>T ENSP00000481376.1:p.Ile20Phe
ENST00000466613.2:n.241A>T
ENST00000475506.1:n.146A>T
ENST00000485515.5:n.217A>T
ENST00000491274.5:c.187A>T ENSP00000480482.1:p.Ile63Phe
NM_003000.2:c.229A>T , LRG_316t1:c.229A>T NP_002991.2:p.Ile77Phe
NM_003000.3:c.229A>T MANE Select NP_002991.2:p.Ile77Phe