Canonical Allele Identifier: CA338272787

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027806-A-T
• MyVariant Identifiers: chr1:g.17354301A>T (hg19) ; chr1:g.17027806A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027806A>T , CM000663.2:g.17027806A>T	GRCh38
NC_000001.10:g.17354301A>T , CM000663.1:g.17354301A>T	GRCh37
NC_000001.9:g.17226888A>T	NCBI36
NG_012340.1:g.31365T>A , LRG_316:g.31365T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.312T>A	ENSP00000481376.2:p.Asp104Glu
ENST00000491274.6:c.441T>A	ENSP00000480482.2:p.Asp147Glu
ENST00000375499.8:c.483T>A MANE Select	ENSP00000364649.3:p.Asp161Glu
ENST00000375499.7:c.483T>A	ENSP00000364649.3:p.Asp161Glu
ENST00000463045.2:c.312T>A	ENSP00000481376.1:p.Asp104Glu
ENST00000475506.1:n.400T>A
ENST00000485515.5:n.417T>A
ENST00000491274.5:c.441T>A	ENSP00000480482.1:p.Asp147Glu
NM_003000.2:c.483T>A , LRG_316t1:c.483T>A	NP_002991.2:p.Asp161Glu
NM_003000.3:c.483T>A MANE Select	NP_002991.2:p.Asp161Glu