Canonical Allele Identifier: CA2643677448
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17027601-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027601G>T , CM000663.2:g.17027601G>T GRCh38
NC_000001.10:g.17354096G>T , CM000663.1:g.17354096G>T GRCh37
NC_000001.9:g.17226683G>T NCBI36
NG_012340.1:g.31570C>A , LRG_316:g.31570C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+148C>A ENSP00000481376.2:n.369+148C>A
ENST00000491274.6:c.498+148C>A ENSP00000480482.2:n.498+148C>A
ENST00000375499.8:c.540+148C>A MANE Select ENSP00000364649.3:n.540+148C>A
ENST00000375499.7:c.540+148C>A ENSP00000364649.3:n.540+148C>A
ENST00000485515.5:n.474+148C>A
ENST00000491274.5:c.498+148C>A ENSP00000480482.1:n.498+148C>A
NM_003000.2:c.540+148C>A , LRG_316t1:c.540+148C>A NP_002991.2:n.540+148C>A
NM_003000.3:c.540+148C>A MANE Select NP_002991.2:n.540+148C>A
Search 100 bp 5'
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