Canonical Allele Identifier: CA2643678157

Gene: SDHB

Linked Data

• gnomAD v4: 1-17028764-C-CTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028765_17028767dup , CM000663.2:g.17028765_17028767dup	GRCh38
NC_000001.10:g.17355260_17355262dup , CM000663.1:g.17355260_17355262dup	GRCh37
NC_000001.9:g.17227847_17227849dup	NCBI36
NG_012340.1:g.30404_30406dup , LRG_316:g.30404_30406dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.116-31_116-29dup	ENSP00000481376.2:n.116-31_116-29dup
ENST00000491274.6:c.245-31_245-29dup	ENSP00000480482.2:n.245-31_245-29dup
ENST00000375499.8:c.287-31_287-29dup MANE Select	ENSP00000364649.3:n.287-31_287-29dup
ENST00000375499.7:c.287-31_287-29dup	ENSP00000364649.3:n.287-31_287-29dup
ENST00000463045.2:c.116-31_116-29dup	ENSP00000481376.1:n.116-31_116-29dup
ENST00000475506.1:n.204-31_204-29dup
ENST00000485515.5:n.275-31_275-29dup
ENST00000491274.5:c.245-31_245-29dup	ENSP00000480482.1:n.245-31_245-29dup
NM_003000.2:c.287-31_287-29dup , LRG_316t1:c.287-31_287-29dup	NP_002991.2:n.287-31_287-29dup
NM_003000.3:c.287-31_287-29dup MANE Select	NP_002991.2:n.287-31_287-29dup