Canonical Allele Identifier: CA338270255

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349155A>T (hg19) ; chr1:g.17022660A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022660A>T , CM000663.2:g.17022660A>T	GRCh38
NC_000001.10:g.17349155A>T , CM000663.1:g.17349155A>T	GRCh37
NC_000001.9:g.17221742A>T	NCBI36
NG_012340.1:g.36511T>A , LRG_316:g.36511T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.542T>A	ENSP00000481376.2:p.Phe181Tyr
ENST00000491274.6:c.671T>A	ENSP00000480482.2:p.Phe224Tyr
ENST00000375499.8:c.713T>A MANE Select	ENSP00000364649.3:p.Phe238Tyr
ENST00000375499.7:c.713T>A	ENSP00000364649.3:p.Phe238Tyr
ENST00000475049.5:n.138T>A
ENST00000485092.5:n.377T>A
ENST00000485515.5:n.647T>A
NM_003000.2:c.713T>A , LRG_316t1:c.713T>A	NP_002991.2:p.Phe238Tyr
NM_003000.3:c.713T>A MANE Select	NP_002991.2:p.Phe238Tyr