Canonical Allele Identifier: CA089577
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 417298
dbSNP Id: rs200419171
gnomAD v2: 1-17355235-A-G
gnomAD v3: 1-17028740-A-G
gnomAD v4: 1-17028740-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028740A>G , CM000663.2:g.17028740A>G GRCh38
NC_000001.10:g.17355235A>G , CM000663.1:g.17355235A>G GRCh37
NC_000001.9:g.17227822A>G NCBI36
NG_012340.1:g.30431T>C , LRG_316:g.30431T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.116-4T>C ENSP00000481376.2:n.116-4T>C
ENST00000491274.6:c.245-4T>C ENSP00000480482.2:n.245-4T>C
ENST00000375499.8:c.287-4T>C MANE Select ENSP00000364649.3:n.287-4T>C
ENST00000375499.7:c.287-4T>C ENSP00000364649.3:n.287-4T>C
ENST00000463045.2:c.116-4T>C ENSP00000481376.1:n.116-4T>C
ENST00000475506.1:n.204-4T>C
ENST00000485515.5:n.275-4T>C
ENST00000491274.5:c.245-4T>C ENSP00000480482.1:n.245-4T>C
NM_003000.2:c.287-4T>C , LRG_316t1:c.287-4T>C NP_002991.2:n.287-4T>C
NM_003000.3:c.287-4T>C MANE Select NP_002991.2:n.287-4T>C