Canonical Allele Identifier: CA890984765

Gene: SDHB

Linked Data

• dbSNP Id: rs1380607179
• gnomAD v3: 1-17022346-G-GT
• gnomAD v4: 1-17022346-G-GT
• MyVariant Identifiers: chr1:g.17348841_17348842insT (hg19) ; chr1:g.17022346_17022347insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022348dup , CM000663.2:g.17022348dup	GRCh38
NC_000001.10:g.17348843dup , CM000663.1:g.17348843dup	GRCh37
NC_000001.9:g.17221430dup	NCBI36
NG_012340.1:g.36824dup , LRG_316:g.36824dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+261dup	ENSP00000481376.2:n.594+261dup
ENST00000491274.6:c.723+261dup	ENSP00000480482.2:n.723+261dup
ENST00000375499.8:c.765+261dup MANE Select	ENSP00000364649.3:n.765+261dup
ENST00000375499.7:c.765+261dup	ENSP00000364649.3:n.765+261dup
ENST00000475049.5:n.190+261dup
ENST00000485092.5:n.429+261dup
NM_003000.2:c.765+261dup , LRG_316t1:c.765+261dup	NP_002991.2:n.765+261dup
NM_003000.3:c.765+261dup MANE Select	NP_002991.2:n.765+261dup