Canonical Allele Identifier: CA2643676144

Gene: SDHB

Linked Data

• gnomAD v4: 1-17022996-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022996A>C , CM000663.2:g.17022996A>C	GRCh38
NC_000001.10:g.17349491A>C , CM000663.1:g.17349491A>C	GRCh37
NC_000001.9:g.17222078A>C	NCBI36
NG_012340.1:g.36175T>G , LRG_316:g.36175T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.472-266T>G	ENSP00000481376.2:n.472-266T>G
ENST00000491274.6:c.601-266T>G	ENSP00000480482.2:n.601-266T>G
ENST00000375499.8:c.643-266T>G MANE Select	ENSP00000364649.3:n.643-266T>G
ENST00000375499.7:c.643-266T>G	ENSP00000364649.3:n.643-266T>G
ENST00000475049.5:n.67+98T>G
ENST00000485092.5:n.41T>G
ENST00000485515.5:n.577-266T>G
NM_003000.2:c.643-266T>G , LRG_316t1:c.643-266T>G	NP_002991.2:n.643-266T>G
NM_003000.3:c.643-266T>G MANE Select	NP_002991.2:n.643-266T>G