Canonical Allele Identifier: CA2643678700
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17028546-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028546T>G , CM000663.2:g.17028546T>G GRCh38
NC_000001.10:g.17355041T>G , CM000663.1:g.17355041T>G GRCh37
NC_000001.9:g.17227628T>G NCBI36
NG_012340.1:g.30625A>C , LRG_316:g.30625A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+54A>C ENSP00000481376.2:n.252+54A>C
ENST00000491274.6:c.381+54A>C ENSP00000480482.2:n.381+54A>C
ENST00000375499.8:c.423+54A>C MANE Select ENSP00000364649.3:n.423+54A>C
ENST00000375499.7:c.423+54A>C ENSP00000364649.3:n.423+54A>C
ENST00000463045.2:c.252+54A>C ENSP00000481376.1:n.252+54A>C
ENST00000475506.1:n.340+54A>C
ENST00000485515.5:n.357+108A>C
ENST00000491274.5:c.381+54A>C ENSP00000480482.1:n.381+54A>C
NM_003000.2:c.423+54A>C , LRG_316t1:c.423+54A>C NP_002991.2:n.423+54A>C
NM_003000.3:c.423+54A>C MANE Select NP_002991.2:n.423+54A>C
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