Canonical Allele Identifier: CA338230606
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17380447A>T (hg19) chr1:g.17053952A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053952A>T , CM000663.2:g.17053952A>T GRCh38
NC_000001.10:g.17380447A>T , CM000663.1:g.17380447A>T GRCh37
NC_000001.9:g.17253034A>T NCBI36
NG_012340.1:g.5219T>A , LRG_316:g.5219T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.68T>A MANE Select ENSP00000364649.3:p.Leu23Gln
ENST00000375499.7:c.68T>A ENSP00000364649.3:p.Leu23Gln
ENST00000466613.2:n.80T>A
ENST00000485515.5:n.56T>A
NM_003000.2:c.68T>A , LRG_316t1:c.68T>A NP_002991.2:p.Leu23Gln
NM_003000.3:c.68T>A MANE Select NP_002991.2:p.Leu23Gln
Search 100 bp 5'
Search 100 bp 3'