Canonical Allele Identifier: CA999081713

Gene: SDHB

Linked Data

• dbSNP Id: rs2077967244
• gnomAD v3: 1-17022505-C-CAAAT
• gnomAD v4: 1-17022505-C-CAAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022506_17022509dup , CM000663.2:g.17022506_17022509dup	GRCh38
NC_000001.10:g.17349001_17349004dup , CM000663.1:g.17349001_17349004dup	GRCh37
NC_000001.9:g.17221588_17221591dup	NCBI36
NG_012340.1:g.36662_36665dup , LRG_316:g.36662_36665dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+99_594+102dup	ENSP00000481376.2:n.594+99_594+102dup
ENST00000491274.6:c.723+99_723+102dup	ENSP00000480482.2:n.723+99_723+102dup
ENST00000375499.8:c.765+99_765+102dup MANE Select	ENSP00000364649.3:n.765+99_765+102dup
ENST00000375499.7:c.765+99_765+102dup	ENSP00000364649.3:n.765+99_765+102dup
ENST00000475049.5:n.190+99_190+102dup
ENST00000485092.5:n.429+99_429+102dup
NM_003000.2:c.765+99_765+102dup , LRG_316t1:c.765+99_765+102dup	NP_002991.2:n.765+99_765+102dup
NM_003000.3:c.765+99_765+102dup MANE Select	NP_002991.2:n.765+99_765+102dup