Canonical Allele Identifier: CA338272579

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354272A>T (hg19) ; chr1:g.17027777A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027777A>T , CM000663.2:g.17027777A>T	GRCh38
NC_000001.10:g.17354272A>T , CM000663.1:g.17354272A>T	GRCh37
NC_000001.9:g.17226859A>T	NCBI36
NG_012340.1:g.31394T>A , LRG_316:g.31394T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.341T>A	ENSP00000481376.2:p.Leu114Gln
ENST00000491274.6:c.470T>A	ENSP00000480482.2:p.Leu157Gln
ENST00000375499.8:c.512T>A MANE Select	ENSP00000364649.3:p.Leu171Gln
ENST00000375499.7:c.512T>A	ENSP00000364649.3:p.Leu171Gln
ENST00000463045.2:c.341T>A	ENSP00000481376.1:p.Leu114Gln
ENST00000475506.1:n.429T>A
ENST00000485515.5:n.446T>A
ENST00000491274.5:c.470T>A	ENSP00000480482.1:p.Leu157Gln
NM_003000.2:c.512T>A , LRG_316t1:c.512T>A	NP_002991.2:p.Leu171Gln
NM_003000.3:c.512T>A MANE Select	NP_002991.2:p.Leu171Gln