Canonical Allele Identifier: CA338230582
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17380443C>A (hg19) chr1:g.17053948C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053948C>A , CM000663.2:g.17053948C>A GRCh38
NC_000001.10:g.17380443C>A , CM000663.1:g.17380443C>A GRCh37
NC_000001.9:g.17253030C>A NCBI36
NG_012340.1:g.5223G>T , LRG_316:g.5223G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.72G>T MANE Select ENSP00000364649.3:p.Gln24His
ENST00000375499.7:c.72G>T ENSP00000364649.3:p.Gln24His
ENST00000466613.2:n.84G>T
ENST00000485515.5:n.60G>T
NM_003000.2:c.72G>T , LRG_316t1:c.72G>T NP_002991.2:p.Gln24His
NM_003000.3:c.72G>T MANE Select NP_002991.2:p.Gln24His
Search 100 bp 5'
Search 100 bp 3'