Canonical Allele Identifier: CA18666335
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs985769729
MyVariant Identifiers: chr1:g.17354765A>T (hg19) chr1:g.17028270A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028270A>T , CM000663.2:g.17028270A>T GRCh38
NC_000001.10:g.17354765A>T , CM000663.1:g.17354765A>T GRCh37
NC_000001.9:g.17227352A>T NCBI36
NG_012340.1:g.30901T>A , LRG_316:g.30901T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+330T>A ENSP00000481376.2:n.252+330T>A
ENST00000491274.6:c.381+330T>A ENSP00000480482.2:n.381+330T>A
ENST00000375499.8:c.423+330T>A MANE Select ENSP00000364649.3:n.423+330T>A
ENST00000375499.7:c.423+330T>A ENSP00000364649.3:n.423+330T>A
ENST00000463045.2:c.252+330T>A ENSP00000481376.1:n.252+330T>A
ENST00000475506.1:n.340+330T>A
ENST00000485515.5:n.357+384T>A
ENST00000491274.5:c.381+330T>A ENSP00000480482.1:n.381+330T>A
NM_003000.2:c.423+330T>A , LRG_316t1:c.423+330T>A NP_002991.2:n.423+330T>A
NM_003000.3:c.423+330T>A MANE Select NP_002991.2:n.423+330T>A
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