Canonical Allele Identifier: CA416087675
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17355143T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028648T>A , CM000663.2:g.17028648T>A GRCh38
NC_000001.10:g.17355143T>A , CM000663.1:g.17355143T>A GRCh37
NC_000001.9:g.17227730T>A NCBI36
NG_012340.1:g.30523A>T , LRG_316:g.30523A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.204A>T ENSP00000481376.2:p.Ser68=
ENST00000491274.6:c.333A>T ENSP00000480482.2:p.Ser111=
ENST00000375499.8:c.375A>T MANE Select ENSP00000364649.3:p.Ser125=
ENST00000375499.7:c.375A>T ENSP00000364649.3:p.Ser125=
ENST00000463045.2:c.204A>T ENSP00000481376.1:p.Ser68=
ENST00000475506.1:n.292A>T
ENST00000485515.5:n.357+6A>T
ENST00000491274.5:c.333A>T ENSP00000480482.1:p.Ser111=
NM_003000.2:c.375A>T , LRG_316t1:c.375A>T NP_002991.2:p.Ser125=
NM_003000.3:c.375A>T MANE Select NP_002991.2:p.Ser125=