Canonical Allele Identifier: CA890972341

Gene: SDHB

Linked Data

• dbSNP Id: rs1196147372
• MyVariant Identifiers: chr1:g.17355000_17355001insA (hg19) ; chr1:g.17028505_17028506insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028508dup , CM000663.2:g.17028508dup	GRCh38
NC_000001.10:g.17355003dup , CM000663.1:g.17355003dup	GRCh37
NC_000001.9:g.17227590dup	NCBI36
NG_012340.1:g.30665dup , LRG_316:g.30665dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+94dup	ENSP00000481376.2:n.252+94dup
ENST00000491274.6:c.381+94dup	ENSP00000480482.2:n.381+94dup
ENST00000375499.8:c.423+94dup MANE Select	ENSP00000364649.3:n.423+94dup
ENST00000375499.7:c.423+94dup	ENSP00000364649.3:n.423+94dup
ENST00000463045.2:c.252+94dup	ENSP00000481376.1:n.252+94dup
ENST00000475506.1:n.340+94dup
ENST00000485515.5:n.357+148dup
ENST00000491274.5:c.381+94dup	ENSP00000480482.1:n.381+94dup
NM_003000.2:c.423+94dup , LRG_316t1:c.423+94dup	NP_002991.2:n.423+94dup
NM_003000.3:c.423+94dup MANE Select	NP_002991.2:n.423+94dup