Canonical Allele Identifier: CA915941152

Gene: SDHB

Linked Data

• ClinVar Variation Id: 754987
• ClinVar RCV Id: RCV001451649
• dbSNP Id: rs1570944969

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022734dup , CM000663.2:g.17022734dup	GRCh38
NC_000001.10:g.17349229dup , CM000663.1:g.17349229dup	GRCh37
NC_000001.9:g.17221816dup	NCBI36
NG_012340.1:g.36438dup , LRG_316:g.36438dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.472-3dup	ENSP00000481376.2:n.472-3dup
ENST00000491274.6:c.601-3dup	ENSP00000480482.2:n.601-3dup
ENST00000375499.8:c.643-3dup MANE Select	ENSP00000364649.3:n.643-3dup
ENST00000375499.7:c.643-3dup	ENSP00000364649.3:n.643-3dup
ENST00000475049.5:n.68-3dup
ENST00000485092.5:n.304dup
ENST00000485515.5:n.577-3dup
NM_003000.2:c.643-3dup , LRG_316t1:c.643-3dup	NP_002991.2:n.643-3dup
NM_003000.3:c.643-3dup MANE Select	NP_002991.2:n.643-3dup