Canonical Allele Identifier: CA2643678693
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2101522798
gnomAD v4: 1-17028544-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028544C>T , CM000663.2:g.17028544C>T GRCh38
NC_000001.10:g.17355039C>T , CM000663.1:g.17355039C>T GRCh37
NC_000001.9:g.17227626C>T NCBI36
NG_012340.1:g.30627G>A , LRG_316:g.30627G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+56G>A ENSP00000481376.2:n.252+56G>A
ENST00000491274.6:c.381+56G>A ENSP00000480482.2:n.381+56G>A
ENST00000375499.8:c.423+56G>A MANE Select ENSP00000364649.3:n.423+56G>A
ENST00000375499.7:c.423+56G>A ENSP00000364649.3:n.423+56G>A
ENST00000463045.2:c.252+56G>A ENSP00000481376.1:n.252+56G>A
ENST00000475506.1:n.340+56G>A
ENST00000485515.5:n.357+110G>A
ENST00000491274.5:c.381+56G>A ENSP00000480482.1:n.381+56G>A
NM_003000.2:c.423+56G>A , LRG_316t1:c.423+56G>A NP_002991.2:n.423+56G>A
NM_003000.3:c.423+56G>A MANE Select NP_002991.2:n.423+56G>A
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