Canonical Allele Identifier: CA2643678142

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027872-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027872T>C , CM000663.2:g.17027872T>C	GRCh38
NC_000001.10:g.17354367T>C , CM000663.1:g.17354367T>C	GRCh37
NC_000001.9:g.17226954T>C	NCBI36
NG_012340.1:g.31299A>G , LRG_316:g.31299A>G

Transcript Alleles

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