Canonical Allele Identifier: CA890972301

Gene: SDHB

Linked Data

• dbSNP Id: rs1433532268
• gnomAD v3: 1-17028133-C-T
• gnomAD v4: 1-17028133-C-T
• MyVariant Identifiers: chr1:g.17354628C>T (hg19) ; chr1:g.17028133C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028133C>T , CM000663.2:g.17028133C>T	GRCh38
NC_000001.10:g.17354628C>T , CM000663.1:g.17354628C>T	GRCh37
NC_000001.9:g.17227215C>T	NCBI36
NG_012340.1:g.31038G>A , LRG_316:g.31038G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-268G>A	ENSP00000481376.2:n.253-268G>A
ENST00000491274.6:c.382-268G>A	ENSP00000480482.2:n.382-268G>A
ENST00000375499.8:c.424-268G>A MANE Select	ENSP00000364649.3:n.424-268G>A
ENST00000375499.7:c.424-268G>A	ENSP00000364649.3:n.424-268G>A
ENST00000463045.2:c.253-268G>A	ENSP00000481376.1:n.253-268G>A
ENST00000475506.1:n.341-268G>A
ENST00000485515.5:n.358-268G>A
ENST00000491274.5:c.382-268G>A	ENSP00000480482.1:n.382-268G>A
NM_003000.2:c.424-268G>A , LRG_316t1:c.424-268G>A	NP_002991.2:n.424-268G>A
NM_003000.3:c.424-268G>A MANE Select	NP_002991.2:n.424-268G>A