Canonical Allele Identifier: CA338268983
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 459172
ClinVar RCV Id: RCV000544462

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17018942T>G , CM000663.2:g.17018942T>G GRCh38
NC_000001.10:g.17345437T>G , CM000663.1:g.17345437T>G GRCh37
NC_000001.9:g.17218024T>G NCBI36
NG_012340.1:g.40229A>C , LRG_316:g.40229A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.782A>C MANE Select ENSP00000364649.3:p.Lys261Thr
ENST00000375499.7:c.782A>C ENSP00000364649.3:p.Lys261Thr
ENST00000475049.5:n.207A>C
ENST00000485092.5:n.446A>C
NM_003000.2:c.782A>C , LRG_316t1:c.782A>C NP_002991.2:p.Lys261Thr
NM_003000.3:c.782A>C MANE Select NP_002991.2:p.Lys261Thr