Canonical Allele Identifier: CA2580060645
Gene: SDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 2050274
ClinVar RCV Id: RCV002914436
gnomAD v4: 1-17027733-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027733A>G , CM000663.2:g.17027733A>G GRCh38
NC_000001.10:g.17354228A>G , CM000663.1:g.17354228A>G GRCh37
NC_000001.9:g.17226815A>G NCBI36
NG_012340.1:g.31438T>C , LRG_316:g.31438T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+16T>C ENSP00000481376.2:n.369+16T>C
ENST00000491274.6:c.498+16T>C ENSP00000480482.2:n.498+16T>C
ENST00000375499.8:c.540+16T>C MANE Select ENSP00000364649.3:n.540+16T>C
ENST00000375499.7:c.540+16T>C ENSP00000364649.3:n.540+16T>C
ENST00000475506.1:n.473T>C
ENST00000485515.5:n.474+16T>C
ENST00000491274.5:c.498+16T>C ENSP00000480482.1:n.498+16T>C
NM_003000.2:c.540+16T>C , LRG_316t1:c.540+16T>C NP_002991.2:n.540+16T>C
NM_003000.3:c.540+16T>C MANE Select NP_002991.2:n.540+16T>C
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