Canonical Allele Identifier: CA2695268122
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1311107626
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044909C>G , CM000663.2:g.17044909C>G GRCh38
NC_000001.10:g.17371404C>G , CM000663.1:g.17371404C>G GRCh37
NC_000001.9:g.17243991C>G NCBI36
NG_012340.1:g.14262G>C , LRG_316:g.14262G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.-99-21G>C ENSP00000481376.2:n.-99-21G>C
ENST00000491274.6:c.31-21G>C ENSP00000480482.2:n.31-21G>C
ENST00000375499.8:c.73-21G>C MANE Select ENSP00000364649.3:n.73-21G>C
ENST00000375499.7:c.73-21G>C ENSP00000364649.3:n.73-21G>C
ENST00000463045.2:c.-99-21G>C ENSP00000481376.1:n.-99-21G>C
ENST00000466613.2:n.85-21G>C
ENST00000485515.5:n.61-21G>C
ENST00000491274.5:c.31-21G>C ENSP00000480482.1:n.31-21G>C
NM_003000.2:c.73-21G>C , LRG_316t1:c.73-21G>C NP_002991.2:n.73-21G>C
NM_003000.3:c.73-21G>C MANE Select NP_002991.2:n.73-21G>C
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