Canonical Allele Identifier: CA645372271
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077967205
gnomAD v4: 1-17022492-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022492T>C , CM000663.2:g.17022492T>C GRCh38
NC_000001.10:g.17348987T>C , CM000663.1:g.17348987T>C GRCh37
NC_000001.9:g.17221574T>C NCBI36
NG_012340.1:g.36679A>G , LRG_316:g.36679A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+116A>G ENSP00000481376.2:n.594+116A>G
ENST00000491274.6:c.723+116A>G ENSP00000480482.2:n.723+116A>G
ENST00000375499.8:c.765+116A>G MANE Select ENSP00000364649.3:n.765+116A>G
ENST00000375499.7:c.765+116A>G ENSP00000364649.3:n.765+116A>G
ENST00000475049.5:n.190+116A>G
ENST00000485092.5:n.429+116A>G
NM_003000.2:c.765+116A>G , LRG_316t1:c.765+116A>G NP_002991.2:n.765+116A>G
NM_003000.3:c.765+116A>G MANE Select NP_002991.2:n.765+116A>G
Search 100 bp 5'
Search 100 bp 3'