Canonical Allele Identifier: CA1156080337

Gene: SDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028182_17028184delinsCAT , CM000663.2:g.17028182_17028184delinsCAT	GRCh38
NC_000001.10:g.17354677_17354679delinsCAT , CM000663.1:g.17354677_17354679delinsCAT	GRCh37
NC_000001.9:g.17227264_17227266delinsCAT	NCBI36
NG_012340.1:g.30987_30989delinsATG , LRG_316:g.30987_30989delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-319_253-317delinsATG	ENSP00000481376.2:n.253-319_253-317delinsATG
ENST00000491274.6:c.382-319_382-317delinsATG	ENSP00000480482.2:n.382-319_382-317delinsATG
ENST00000375499.8:c.424-319_424-317delinsATG MANE Select	ENSP00000364649.3:n.424-319_424-317delinsATG
ENST00000375499.7:c.424-319_424-317delinsATG	ENSP00000364649.3:n.424-319_424-317delinsATG
ENST00000463045.2:c.253-319_253-317delinsATG	ENSP00000481376.1:n.253-319_253-317delinsATG
ENST00000475506.1:n.341-319_341-317delinsATG
ENST00000485515.5:n.358-319_358-317delinsATG
ENST00000491274.5:c.382-319_382-317delinsATG	ENSP00000480482.1:n.382-319_382-317delinsATG
NM_003000.2:c.424-319_424-317delinsATG , LRG_316t1:c.424-319_424-317delinsATG	NP_002991.2:n.424-319_424-317delinsATG
NM_003000.3:c.424-319_424-317delinsATG MANE Select	NP_002991.2:n.424-319_424-317delinsATG