Canonical Allele Identifier: CA338272712

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354290T>A (hg19) ; chr1:g.17027795T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027795T>A , CM000663.2:g.17027795T>A	GRCh38
NC_000001.10:g.17354290T>A , CM000663.1:g.17354290T>A	GRCh37
NC_000001.9:g.17226877T>A	NCBI36
NG_012340.1:g.31376A>T , LRG_316:g.31376A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.323A>T	ENSP00000481376.2:p.Glu108Val
ENST00000491274.6:c.452A>T	ENSP00000480482.2:p.Glu151Val
ENST00000375499.8:c.494A>T MANE Select	ENSP00000364649.3:p.Glu165Val
ENST00000375499.7:c.494A>T	ENSP00000364649.3:p.Glu165Val
ENST00000463045.2:c.323A>T	ENSP00000481376.1:p.Glu108Val
ENST00000475506.1:n.411A>T
ENST00000485515.5:n.428A>T
ENST00000491274.5:c.452A>T	ENSP00000480482.1:p.Glu151Val
NM_003000.2:c.494A>T , LRG_316t1:c.494A>T	NP_002991.2:p.Glu165Val
NM_003000.3:c.494A>T MANE Select	NP_002991.2:p.Glu165Val