Canonical Allele Identifier: CA2643677626
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077999115
gnomAD v4: 1-17027737-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027737G>T , CM000663.2:g.17027737G>T GRCh38
NC_000001.10:g.17354232G>T , CM000663.1:g.17354232G>T GRCh37
NC_000001.9:g.17226819G>T NCBI36
NG_012340.1:g.31434C>A , LRG_316:g.31434C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+12C>A ENSP00000481376.2:n.369+12C>A
ENST00000491274.6:c.498+12C>A ENSP00000480482.2:n.498+12C>A
ENST00000375499.8:c.540+12C>A MANE Select ENSP00000364649.3:n.540+12C>A
ENST00000375499.7:c.540+12C>A ENSP00000364649.3:n.540+12C>A
ENST00000475506.1:n.469C>A
ENST00000485515.5:n.474+12C>A
ENST00000491274.5:c.498+12C>A ENSP00000480482.1:n.498+12C>A
NM_003000.2:c.540+12C>A , LRG_316t1:c.540+12C>A NP_002991.2:n.540+12C>A
NM_003000.3:c.540+12C>A MANE Select NP_002991.2:n.540+12C>A
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