Canonical Allele Identifier: CA521039239

Gene: SDHB

Linked Data

• dbSNP Id: rs1355143682
• gnomAD v2: 1-17354629-G-T
• gnomAD v3: 1-17028134-G-T
• gnomAD v4: 1-17028134-G-T
• MyVariant Identifiers: chr1:g.17354629G>T (hg19) ; chr1:g.17028134G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028134G>T , CM000663.2:g.17028134G>T	GRCh38
NC_000001.10:g.17354629G>T , CM000663.1:g.17354629G>T	GRCh37
NC_000001.9:g.17227216G>T	NCBI36
NG_012340.1:g.31037C>A , LRG_316:g.31037C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-269C>A	ENSP00000481376.2:n.253-269C>A
ENST00000491274.6:c.382-269C>A	ENSP00000480482.2:n.382-269C>A
ENST00000375499.8:c.424-269C>A MANE Select	ENSP00000364649.3:n.424-269C>A
ENST00000375499.7:c.424-269C>A	ENSP00000364649.3:n.424-269C>A
ENST00000463045.2:c.253-269C>A	ENSP00000481376.1:n.253-269C>A
ENST00000475506.1:n.341-269C>A
ENST00000485515.5:n.358-269C>A
ENST00000491274.5:c.382-269C>A	ENSP00000480482.1:n.382-269C>A
NM_003000.2:c.424-269C>A , LRG_316t1:c.424-269C>A	NP_002991.2:n.424-269C>A
NM_003000.3:c.424-269C>A MANE Select	NP_002991.2:n.424-269C>A