Canonical Allele Identifier: CA2643675647

Gene: SDHB

Linked Data

• gnomAD v4: 1-17022598-C-CAATAGCTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022598_17022599insAATAGCTTT , CM000663.2:g.17022598_17022599insAATAGCTTT	GRCh38
NC_000001.10:g.17349093_17349094insAATAGCTTT , CM000663.1:g.17349093_17349094insAATAGCTTT	GRCh37
NC_000001.9:g.17221680_17221681insAATAGCTTT	NCBI36
NG_012340.1:g.36572_36573insAAAGCTATT , LRG_316:g.36572_36573insAAAGCTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+9_594+10insAAAGCTATT	ENSP00000481376.2:n.594+9_594+10insAAAGCTATT
ENST00000491274.6:c.723+9_723+10insAAAGCTATT	ENSP00000480482.2:n.723+9_723+10insAAAGCTATT
ENST00000375499.8:c.765+9_765+10insAAAGCTATT MANE Select	ENSP00000364649.3:n.765+9_765+10insAAAGCTATT
ENST00000375499.7:c.765+9_765+10insAAAGCTATT	ENSP00000364649.3:n.765+9_765+10insAAAGCTATT
ENST00000475049.5:n.190+9_190+10insAAAGCTATT
ENST00000485092.5:n.429+9_429+10insAAAGCTATT
NM_003000.2:c.765+9_765+10insAAAGCTATT , LRG_316t1:c.765+9_765+10insAAAGCTATT	NP_002991.2:n.765+9_765+10insAAAGCTATT
NM_003000.3:c.765+9_765+10insAAAGCTATT MANE Select	NP_002991.2:n.765+9_765+10insAAAGCTATT