Canonical Allele Identifier: CA2643675997

Gene: SDHB

Linked Data

• gnomAD v4: 1-17022908-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022908T>C , CM000663.2:g.17022908T>C	GRCh38
NC_000001.10:g.17349403T>C , CM000663.1:g.17349403T>C	GRCh37
NC_000001.9:g.17221990T>C	NCBI36
NG_012340.1:g.36263A>G , LRG_316:g.36263A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.472-178A>G	ENSP00000481376.2:n.472-178A>G
ENST00000491274.6:c.601-178A>G	ENSP00000480482.2:n.601-178A>G
ENST00000375499.8:c.643-178A>G MANE Select	ENSP00000364649.3:n.643-178A>G
ENST00000375499.7:c.643-178A>G	ENSP00000364649.3:n.643-178A>G
ENST00000475049.5:n.68-178A>G
ENST00000485092.5:n.129A>G
ENST00000485515.5:n.577-178A>G
NM_003000.2:c.643-178A>G , LRG_316t1:c.643-178A>G	NP_002991.2:n.643-178A>G
NM_003000.3:c.643-178A>G MANE Select	NP_002991.2:n.643-178A>G