Canonical Allele Identifier: CA1156080338

Gene: SDHB

Linked Data

• dbSNP Id: rs2078002063

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028184_17028185del , CM000663.2:g.17028184_17028185del	GRCh38
NC_000001.10:g.17354679_17354680del , CM000663.1:g.17354679_17354680del	GRCh37
NC_000001.9:g.17227266_17227267del	NCBI36
NG_012340.1:g.30987_30988del , LRG_316:g.30987_30988del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-319_253-318del	ENSP00000481376.2:n.253-319_253-318del
ENST00000491274.6:c.382-319_382-318del	ENSP00000480482.2:n.382-319_382-318del
ENST00000375499.8:c.424-319_424-318del MANE Select	ENSP00000364649.3:n.424-319_424-318del
ENST00000375499.7:c.424-319_424-318del	ENSP00000364649.3:n.424-319_424-318del
ENST00000463045.2:c.253-319_253-318del	ENSP00000481376.1:n.253-319_253-318del
ENST00000475506.1:n.341-319_341-318del
ENST00000485515.5:n.358-319_358-318del
ENST00000491274.5:c.382-319_382-318del	ENSP00000480482.1:n.382-319_382-318del
NM_003000.2:c.424-319_424-318del , LRG_316t1:c.424-319_424-318del	NP_002991.2:n.424-319_424-318del
NM_003000.3:c.424-319_424-318del MANE Select	NP_002991.2:n.424-319_424-318del