Canonical Allele Identifier: CA338276420

Gene: SDHB

Linked Data

• ClinVar Variation Id: 438413
• ClinVar RCV Id: RCV000505298
• dbSNP Id: rs1553178040
• MyVariant Identifiers: chr1:g.17359566G>T (hg19) ; chr1:g.17033071G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17033071G>T , CM000663.2:g.17033071G>T	GRCh38
NC_000001.10:g.17359566G>T , CM000663.1:g.17359566G>T	GRCh37
NC_000001.9:g.17232153G>T	NCBI36
NG_012340.1:g.26100C>A , LRG_316:g.26100C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.104C>A	ENSP00000481376.2:p.Ser35Ter
ENST00000491274.6:c.233C>A	ENSP00000480482.2:p.Ser78Ter
ENST00000375499.8:c.275C>A MANE Select	ENSP00000364649.3:p.Ser92Ter
ENST00000375499.7:c.275C>A	ENSP00000364649.3:p.Ser92Ter
ENST00000463045.2:c.104C>A	ENSP00000481376.1:p.Ser35Ter
ENST00000466613.2:n.287C>A
ENST00000475506.1:n.192C>A
ENST00000485515.5:n.263C>A
ENST00000491274.5:c.233C>A	ENSP00000480482.1:p.Ser78Ter
NM_003000.2:c.275C>A , LRG_316t1:c.275C>A	NP_002991.2:p.Ser92Ter
NM_003000.3:c.275C>A MANE Select	NP_002991.2:p.Ser92Ter