Canonical Allele Identifier: CA338272829
Gene: SDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027810T>C , CM000663.2:g.17027810T>C GRCh38
NC_000001.10:g.17354305T>C , CM000663.1:g.17354305T>C GRCh37
NC_000001.9:g.17226892T>C NCBI36
NG_012340.1:g.31361A>G , LRG_316:g.31361A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.308A>G ENSP00000481376.2:p.Lys103Arg
ENST00000491274.6:c.437A>G ENSP00000480482.2:p.Lys146Arg
ENST00000375499.8:c.479A>G MANE Select ENSP00000364649.3:p.Lys160Arg
ENST00000375499.7:c.479A>G ENSP00000364649.3:p.Lys160Arg
ENST00000463045.2:c.308A>G ENSP00000481376.1:p.Lys103Arg
ENST00000475506.1:n.396A>G
ENST00000485515.5:n.413A>G
ENST00000491274.5:c.437A>G ENSP00000480482.1:p.Lys146Arg
NM_003000.2:c.479A>G , LRG_316t1:c.479A>G NP_002991.2:p.Lys160Arg
NM_003000.3:c.479A>G MANE Select NP_002991.2:p.Lys160Arg