Canonical Allele Identifier: CA1156077800
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077965728
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022213A>G , CM000663.2:g.17022213A>G GRCh38
NC_000001.10:g.17348708A>G , CM000663.1:g.17348708A>G GRCh37
NC_000001.9:g.17221295A>G NCBI36
NG_012340.1:g.36958T>C , LRG_316:g.36958T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+395T>C ENSP00000481376.2:n.594+395T>C
ENST00000491274.6:c.723+395T>C ENSP00000480482.2:n.723+395T>C
ENST00000375499.8:c.765+395T>C MANE Select ENSP00000364649.3:n.765+395T>C
ENST00000375499.7:c.765+395T>C ENSP00000364649.3:n.765+395T>C
ENST00000475049.5:n.190+395T>C
ENST00000485092.5:n.429+395T>C
NM_003000.2:c.765+395T>C , LRG_316t1:c.765+395T>C NP_002991.2:n.765+395T>C
NM_003000.3:c.765+395T>C MANE Select NP_002991.2:n.765+395T>C
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