Canonical Allele Identifier: CA416081934
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17349153_17349157del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022658_17022662del , CM000663.2:g.17022658_17022662del GRCh38
NC_000001.10:g.17349153_17349157del , CM000663.1:g.17349153_17349157del GRCh37
NC_000001.9:g.17221740_17221744del NCBI36
NG_012340.1:g.36509_36513del , LRG_316:g.36509_36513del

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.540_544del ENSP00000481376.2:p.Phe181SerfsTer16
ENST00000491274.6:c.669_673del ENSP00000480482.2:p.Phe224SerfsTer16
ENST00000375499.8:c.711_715del MANE Select ENSP00000364649.3:p.Phe238SerfsTer16
ENST00000375499.7:c.711_715del ENSP00000364649.3:p.Phe238SerfsTer16
ENST00000475049.5:n.136_140del
ENST00000485092.5:n.375_379del
ENST00000485515.5:n.645_649del
NM_003000.2:c.711_715del , LRG_316t1:c.711_715del NP_002991.2:p.Phe238SerfsTer16
NM_003000.3:c.711_715del MANE Select NP_002991.2:p.Phe238SerfsTer16
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