Canonical Allele Identifier: CA2574235777

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1934679
• ClinVar RCV Id: RCV002638788
• gnomAD v4: 1-17027873-TAAGAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027878_17027883del , CM000663.2:g.17027878_17027883del	GRCh38
NC_000001.10:g.17354373_17354378del , CM000663.1:g.17354373_17354378del	GRCh37
NC_000001.9:g.17226960_17226965del	NCBI36
NG_012340.1:g.31292_31297del , LRG_316:g.31292_31297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-14_253-9del	ENSP00000481376.2:n.253-14_253-9del
ENST00000491274.6:c.382-14_382-9del	ENSP00000480482.2:n.382-14_382-9del
ENST00000375499.8:c.424-14_424-9del MANE Select	ENSP00000364649.3:n.424-14_424-9del
ENST00000375499.7:c.424-14_424-9del	ENSP00000364649.3:n.424-14_424-9del
ENST00000463045.2:c.253-14_253-9del	ENSP00000481376.1:n.253-14_253-9del
ENST00000475506.1:n.341-14_341-9del
ENST00000485515.5:n.358-14_358-9del
ENST00000491274.5:c.382-14_382-9del	ENSP00000480482.1:n.382-14_382-9del
NM_003000.2:c.424-14_424-9del , LRG_316t1:c.424-14_424-9del	NP_002991.2:n.424-14_424-9del
NM_003000.3:c.424-14_424-9del MANE Select	NP_002991.2:n.424-14_424-9del