Canonical Allele Identifier: CA338273397

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1358962
• ClinVar RCV Id: RCV001904292
• dbSNP Id: rs2101521886
• MyVariant Identifiers: chr1:g.17354347A>G (hg19) ; chr1:g.17027852A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027852A>G , CM000663.2:g.17027852A>G	GRCh38
NC_000001.10:g.17354347A>G , CM000663.1:g.17354347A>G	GRCh37
NC_000001.9:g.17226934A>G	NCBI36
NG_012340.1:g.31319T>C , LRG_316:g.31319T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.266T>C	ENSP00000481376.2:p.Phe89Ser
ENST00000491274.6:c.395T>C	ENSP00000480482.2:p.Phe132Ser
ENST00000375499.8:c.437T>C MANE Select	ENSP00000364649.3:p.Phe146Ser
ENST00000375499.7:c.437T>C	ENSP00000364649.3:p.Phe146Ser
ENST00000463045.2:c.266T>C	ENSP00000481376.1:p.Phe89Ser
ENST00000475506.1:n.354T>C
ENST00000485515.5:n.371T>C
ENST00000491274.5:c.395T>C	ENSP00000480482.1:p.Phe132Ser
NM_003000.2:c.437T>C , LRG_316t1:c.437T>C	NP_002991.2:p.Phe146Ser
NM_003000.3:c.437T>C MANE Select	NP_002991.2:p.Phe146Ser