Canonical Allele Identifier: CA338270494
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 480794
dbSNP Id: rs1553177290

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022720C>G , CM000663.2:g.17022720C>G GRCh38
NC_000001.10:g.17349215C>G , CM000663.1:g.17349215C>G GRCh37
NC_000001.9:g.17221802C>G NCBI36
NG_012340.1:g.36451G>C , LRG_316:g.36451G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.482G>C ENSP00000481376.2:p.Trp161Ser
ENST00000491274.6:c.611G>C ENSP00000480482.2:p.Trp204Ser
ENST00000375499.8:c.653G>C MANE Select ENSP00000364649.3:p.Trp218Ser
ENST00000375499.7:c.653G>C ENSP00000364649.3:p.Trp218Ser
ENST00000475049.5:n.78G>C
ENST00000485092.5:n.317G>C
ENST00000485515.5:n.587G>C
NM_003000.2:c.653G>C , LRG_316t1:c.653G>C NP_002991.2:p.Trp218Ser
NM_003000.3:c.653G>C MANE Select NP_002991.2:p.Trp218Ser