Canonical Allele Identifier: CA338270051

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349123A>T (hg19) ; chr1:g.17022628A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022628A>T , CM000663.2:g.17022628A>T	GRCh38
NC_000001.10:g.17349123A>T , CM000663.1:g.17349123A>T	GRCh37
NC_000001.9:g.17221710A>T	NCBI36
NG_012340.1:g.36543T>A , LRG_316:g.36543T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.574T>A	ENSP00000481376.2:p.Cys192Ser
ENST00000491274.6:c.703T>A	ENSP00000480482.2:p.Cys235Ser
ENST00000375499.8:c.745T>A MANE Select	ENSP00000364649.3:p.Cys249Ser
ENST00000375499.7:c.745T>A	ENSP00000364649.3:p.Cys249Ser
ENST00000475049.5:n.170T>A
ENST00000485092.5:n.409T>A
ENST00000485515.5:n.679T>A
NM_003000.2:c.745T>A , LRG_316t1:c.745T>A	NP_002991.2:p.Cys249Ser
NM_003000.3:c.745T>A MANE Select	NP_002991.2:p.Cys249Ser