Canonical Allele Identifier: CA1156078143
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077970754

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023001T>C , CM000663.2:g.17023001T>C GRCh38
NC_000001.10:g.17349496T>C , CM000663.1:g.17349496T>C GRCh37
NC_000001.9:g.17222083T>C NCBI36
NG_012340.1:g.36170A>G , LRG_316:g.36170A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-271A>G ENSP00000481376.2:n.472-271A>G
ENST00000491274.6:c.601-271A>G ENSP00000480482.2:n.601-271A>G
ENST00000375499.8:c.643-271A>G MANE Select ENSP00000364649.3:n.643-271A>G
ENST00000375499.7:c.643-271A>G ENSP00000364649.3:n.643-271A>G
ENST00000475049.5:n.67+93A>G
ENST00000485092.5:n.36A>G
ENST00000485515.5:n.577-271A>G
NM_003000.2:c.643-271A>G , LRG_316t1:c.643-271A>G NP_002991.2:n.643-271A>G
NM_003000.3:c.643-271A>G MANE Select NP_002991.2:n.643-271A>G