Canonical Allele Identifier: CA18662475
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs962380210
gnomAD v3: 1-17023008-T-G
gnomAD v4: 1-17023008-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17023008T>G , CM000663.2:g.17023008T>G GRCh38
NC_000001.10:g.17349503T>G , CM000663.1:g.17349503T>G GRCh37
NC_000001.9:g.17222090T>G NCBI36
NG_012340.1:g.36163A>C , LRG_316:g.36163A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-278A>C ENSP00000481376.2:n.472-278A>C
ENST00000491274.6:c.601-278A>C ENSP00000480482.2:n.601-278A>C
ENST00000375499.8:c.643-278A>C MANE Select ENSP00000364649.3:n.643-278A>C
ENST00000375499.7:c.643-278A>C ENSP00000364649.3:n.643-278A>C
ENST00000475049.5:n.67+86A>C
ENST00000485092.5:n.29A>C
ENST00000485515.5:n.577-278A>C
NM_003000.2:c.643-278A>C , LRG_316t1:c.643-278A>C NP_002991.2:n.643-278A>C
NM_003000.3:c.643-278A>C MANE Select NP_002991.2:n.643-278A>C