Canonical Allele Identifier: CA338271125
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17350520G>T (hg19) chr1:g.17024025G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17024025G>T , CM000663.2:g.17024025G>T GRCh38
NC_000001.10:g.17350520G>T , CM000663.1:g.17350520G>T GRCh37
NC_000001.9:g.17223107G>T NCBI36
NG_012340.1:g.35146C>A , LRG_316:g.35146C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.419C>A ENSP00000481376.2:p.Pro140His
ENST00000491274.6:c.548C>A ENSP00000480482.2:p.Pro183His
ENST00000375499.8:c.590C>A MANE Select ENSP00000364649.3:p.Pro197His
ENST00000375499.7:c.590C>A ENSP00000364649.3:p.Pro197His
ENST00000485515.5:n.524C>A
ENST00000491274.5:c.548C>A ENSP00000480482.1:p.Pro183His
NM_003000.2:c.590C>A , LRG_316t1:c.590C>A NP_002991.2:p.Pro197His
NM_003000.3:c.590C>A MANE Select NP_002991.2:p.Pro197His
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