Canonical Allele Identifier: CA015853
Gene: SDHB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18454
dbSNP Id: rs267607032

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028605C>A , CM000663.2:g.17028605C>A GRCh38
NC_000001.10:g.17355100C>A , CM000663.1:g.17355100C>A GRCh37
NC_000001.9:g.17227687C>A NCBI36
NG_012340.1:g.30566G>T , LRG_316:g.30566G>T

Transcript Alleles

HGVS Amino-acid change
NM_003000.2:c.418G>T , LRG_316t1:c.418G>T NP_002991.2:p.Val140Phe
ENST00000375499.7:c.418G>T ENSP00000364649.3:p.Val140Phe
ENST00000463045.2:c.247G>T ENSP00000481376.1:p.Val83Phe
ENST00000475506.1:n.335G>T
ENST00000485515.5:n.357+49G>T
ENST00000491274.5:c.376G>T ENSP00000480482.1:p.Val126Phe