Canonical Allele Identifier: CA338273943

Gene: SDHB

Linked Data

• ClinVar Variation Id: 659740
• ClinVar RCV Id: RCV000816787
• dbSNP Id: rs1570948527
• MyVariant Identifiers: chr1:g.17355105T>C (hg19) ; chr1:g.17028610T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028610T>C , CM000663.2:g.17028610T>C	GRCh38
NC_000001.10:g.17355105T>C , CM000663.1:g.17355105T>C	GRCh37
NC_000001.9:g.17227692T>C	NCBI36
NG_012340.1:g.30561A>G , LRG_316:g.30561A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.242A>G	ENSP00000481376.2:p.Asp81Gly
ENST00000491274.6:c.371A>G	ENSP00000480482.2:p.Asp124Gly
ENST00000375499.8:c.413A>G MANE Select	ENSP00000364649.3:p.Asp138Gly
ENST00000375499.7:c.413A>G	ENSP00000364649.3:p.Asp138Gly
ENST00000463045.2:c.242A>G	ENSP00000481376.1:p.Asp81Gly
ENST00000475506.1:n.330A>G
ENST00000485515.5:n.357+44A>G
ENST00000491274.5:c.371A>G	ENSP00000480482.1:p.Asp124Gly
NM_003000.2:c.413A>G , LRG_316t1:c.413A>G	NP_002991.2:p.Asp138Gly
NM_003000.3:c.413A>G MANE Select	NP_002991.2:p.Asp138Gly