Canonical Allele Identifier: CA1156080421

Gene: SDHB

Linked Data

• dbSNP Id: rs2078003332

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028439_17028441dup , CM000663.2:g.17028439_17028441dup	GRCh38
NC_000001.10:g.17354934_17354936dup , CM000663.1:g.17354934_17354936dup	GRCh37
NC_000001.9:g.17227521_17227523dup	NCBI36
NG_012340.1:g.30737_30739dup , LRG_316:g.30737_30739dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+166_252+168dup	ENSP00000481376.2:n.252+166_252+168dup
ENST00000491274.6:c.381+166_381+168dup	ENSP00000480482.2:n.381+166_381+168dup
ENST00000375499.8:c.423+166_423+168dup MANE Select	ENSP00000364649.3:n.423+166_423+168dup
ENST00000375499.7:c.423+166_423+168dup	ENSP00000364649.3:n.423+166_423+168dup
ENST00000463045.2:c.252+166_252+168dup	ENSP00000481376.1:n.252+166_252+168dup
ENST00000475506.1:n.340+166_340+168dup
ENST00000485515.5:n.357+220_357+222dup
ENST00000491274.5:c.381+166_381+168dup	ENSP00000480482.1:n.381+166_381+168dup
NM_003000.2:c.423+166_423+168dup , LRG_316t1:c.423+166_423+168dup	NP_002991.2:n.423+166_423+168dup
NM_003000.3:c.423+166_423+168dup MANE Select	NP_002991.2:n.423+166_423+168dup