Canonical Allele Identifier: CA521039235

Gene: SDHB

Linked Data

• dbSNP Id: rs1370391783
• gnomAD v2: 1-17354620-A-G
• gnomAD v3: 1-17028125-A-G
• gnomAD v4: 1-17028125-A-G
• MyVariant Identifiers: chr1:g.17354620A>G (hg19) ; chr1:g.17028125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028125A>G , CM000663.2:g.17028125A>G	GRCh38
NC_000001.10:g.17354620A>G , CM000663.1:g.17354620A>G	GRCh37
NC_000001.9:g.17227207A>G	NCBI36
NG_012340.1:g.31046T>C , LRG_316:g.31046T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-260T>C	ENSP00000481376.2:n.253-260T>C
ENST00000491274.6:c.382-260T>C	ENSP00000480482.2:n.382-260T>C
ENST00000375499.8:c.424-260T>C MANE Select	ENSP00000364649.3:n.424-260T>C
ENST00000375499.7:c.424-260T>C	ENSP00000364649.3:n.424-260T>C
ENST00000463045.2:c.253-260T>C	ENSP00000481376.1:n.253-260T>C
ENST00000475506.1:n.341-260T>C
ENST00000485515.5:n.358-260T>C
ENST00000491274.5:c.382-260T>C	ENSP00000480482.1:n.382-260T>C
NM_003000.2:c.424-260T>C , LRG_316t1:c.424-260T>C	NP_002991.2:n.424-260T>C
NM_003000.3:c.424-260T>C MANE Select	NP_002991.2:n.424-260T>C