Canonical Allele Identifier: CA1156080090
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1570947754
gnomAD v4: 1-17027606-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027606T>G , CM000663.2:g.17027606T>G GRCh38
NC_000001.10:g.17354101T>G , CM000663.1:g.17354101T>G GRCh37
NC_000001.9:g.17226688T>G NCBI36
NG_012340.1:g.31565A>C , LRG_316:g.31565A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+143A>C ENSP00000481376.2:n.369+143A>C
ENST00000491274.6:c.498+143A>C ENSP00000480482.2:n.498+143A>C
ENST00000375499.8:c.540+143A>C MANE Select ENSP00000364649.3:n.540+143A>C
ENST00000375499.7:c.540+143A>C ENSP00000364649.3:n.540+143A>C
ENST00000485515.5:n.474+143A>C
ENST00000491274.5:c.498+143A>C ENSP00000480482.1:n.498+143A>C
NM_003000.2:c.540+143A>C , LRG_316t1:c.540+143A>C NP_002991.2:n.540+143A>C
NM_003000.3:c.540+143A>C MANE Select NP_002991.2:n.540+143A>C
Search 100 bp 5'
Search 100 bp 3'