Canonical Allele Identifier: CA890972310

Gene: SDHB

Linked Data

• dbSNP Id: rs1204079945
• gnomAD v3: 1-17028153-T-A
• gnomAD v4: 1-17028153-T-A
• MyVariant Identifiers: chr1:g.17354648T>A (hg19) ; chr1:g.17028153T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028153T>A , CM000663.2:g.17028153T>A	GRCh38
NC_000001.10:g.17354648T>A , CM000663.1:g.17354648T>A	GRCh37
NC_000001.9:g.17227235T>A	NCBI36
NG_012340.1:g.31018A>T , LRG_316:g.31018A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-288A>T	ENSP00000481376.2:n.253-288A>T
ENST00000491274.6:c.382-288A>T	ENSP00000480482.2:n.382-288A>T
ENST00000375499.8:c.424-288A>T MANE Select	ENSP00000364649.3:n.424-288A>T
ENST00000375499.7:c.424-288A>T	ENSP00000364649.3:n.424-288A>T
ENST00000463045.2:c.253-288A>T	ENSP00000481376.1:n.253-288A>T
ENST00000475506.1:n.341-288A>T
ENST00000485515.5:n.358-288A>T
ENST00000491274.5:c.382-288A>T	ENSP00000480482.1:n.382-288A>T
NM_003000.2:c.424-288A>T , LRG_316t1:c.424-288A>T	NP_002991.2:n.424-288A>T
NM_003000.3:c.424-288A>T MANE Select	NP_002991.2:n.424-288A>T