Canonical Allele Identifier: CA10581752

Gene: SDHB

Linked Data

• ClinVar Variation Id: 239421
• ClinVar RCV Id: RCV000234616
• dbSNP Id: rs878854572
• MyVariant Identifiers: chr1:g.17371330del (hg19) ; chr1:g.17044835del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044837del , CM000663.2:g.17044837del	GRCh38
NC_000001.10:g.17371332del , CM000663.1:g.17371332del	GRCh37
NC_000001.9:g.17243919del	NCBI36
NG_012340.1:g.14336del , LRG_316:g.14336del

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.-46del	ENSP00000481376.2:n.-46del
ENST00000491274.6:c.84del	ENSP00000480482.2:p.Phe28LeufsTer?
ENST00000375499.8:c.126del MANE Select	ENSP00000364649.3:p.Phe42LeufsTer?
ENST00000375499.7:c.126del	ENSP00000364649.3:p.Phe42LeufsTer?
ENST00000463045.2:c.-46del	ENSP00000481376.1:n.-46del
ENST00000466613.2:n.138del
ENST00000475506.1:n.43del
ENST00000485515.5:n.114del
ENST00000491274.5:c.84del	ENSP00000480482.1:p.Phe28LeufsTer?
NM_003000.2:c.126del , LRG_316t1:c.126del	NP_002991.2:p.Phe42LeufsTer?
NM_003000.3:c.126del MANE Select	NP_002991.2:p.Phe42LeufsTer?