Canonical Allele Identifier: CA2643675606

Gene: SDHB

Linked Data

• gnomAD v4: 1-17022581-G-GGAAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022581_17022582insGAAAC , CM000663.2:g.17022581_17022582insGAAAC	GRCh38
NC_000001.10:g.17349076_17349077insGAAAC , CM000663.1:g.17349076_17349077insGAAAC	GRCh37
NC_000001.9:g.17221663_17221664insGAAAC	NCBI36
NG_012340.1:g.36589_36590insGTTTC , LRG_316:g.36589_36590insGTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+26_594+27insGTTTC	ENSP00000481376.2:n.594+26_594+27insGTTTC
ENST00000491274.6:c.723+26_723+27insGTTTC	ENSP00000480482.2:n.723+26_723+27insGTTTC
ENST00000375499.8:c.765+26_765+27insGTTTC MANE Select	ENSP00000364649.3:n.765+26_765+27insGTTTC
ENST00000375499.7:c.765+26_765+27insGTTTC	ENSP00000364649.3:n.765+26_765+27insGTTTC
ENST00000475049.5:n.190+26_190+27insGTTTC
ENST00000485092.5:n.429+26_429+27insGTTTC
NM_003000.2:c.765+26_765+27insGTTTC , LRG_316t1:c.765+26_765+27insGTTTC	NP_002991.2:n.765+26_765+27insGTTTC
NM_003000.3:c.765+26_765+27insGTTTC MANE Select	NP_002991.2:n.765+26_765+27insGTTTC