Canonical Allele Identifier: CA521039237

Gene: SDHB

Linked Data

• dbSNP Id: rs1428354614
• gnomAD v2: 1-17354622-ACAC-A
• gnomAD v3: 1-17028127-ACAC-A
• gnomAD v4: 1-17028127-ACAC-A
• MyVariant Identifiers: chr1:g.17354623_17354625del (hg19) ; chr1:g.17028128_17028130del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028131_17028133del , CM000663.2:g.17028131_17028133del	GRCh38
NC_000001.10:g.17354626_17354628del , CM000663.1:g.17354626_17354628del	GRCh37
NC_000001.9:g.17227213_17227215del	NCBI36
NG_012340.1:g.31041_31043del , LRG_316:g.31041_31043del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-265_253-263del	ENSP00000481376.2:n.253-265_253-263del
ENST00000491274.6:c.382-265_382-263del	ENSP00000480482.2:n.382-265_382-263del
ENST00000375499.8:c.424-265_424-263del MANE Select	ENSP00000364649.3:n.424-265_424-263del
ENST00000375499.7:c.424-265_424-263del	ENSP00000364649.3:n.424-265_424-263del
ENST00000463045.2:c.253-265_253-263del	ENSP00000481376.1:n.253-265_253-263del
ENST00000475506.1:n.341-265_341-263del
ENST00000485515.5:n.358-265_358-263del
ENST00000491274.5:c.382-265_382-263del	ENSP00000480482.1:n.382-265_382-263del
NM_003000.2:c.424-265_424-263del , LRG_316t1:c.424-265_424-263del	NP_002991.2:n.424-265_424-263del
NM_003000.3:c.424-265_424-263del MANE Select	NP_002991.2:n.424-265_424-263del