Canonical Allele Identifier: CA2643678672

Gene: SDHB

Linked Data

• gnomAD v4: 1-17028530-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028532_17028533del , CM000663.2:g.17028532_17028533del	GRCh38
NC_000001.10:g.17355027_17355028del , CM000663.1:g.17355027_17355028del	GRCh37
NC_000001.9:g.17227614_17227615del	NCBI36
NG_012340.1:g.30639_30640del , LRG_316:g.30639_30640del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+68_252+69del	ENSP00000481376.2:n.252+68_252+69del
ENST00000491274.6:c.381+68_381+69del	ENSP00000480482.2:n.381+68_381+69del
ENST00000375499.8:c.423+68_423+69del MANE Select	ENSP00000364649.3:n.423+68_423+69del
ENST00000375499.7:c.423+68_423+69del	ENSP00000364649.3:n.423+68_423+69del
ENST00000463045.2:c.252+68_252+69del	ENSP00000481376.1:n.252+68_252+69del
ENST00000475506.1:n.340+68_340+69del
ENST00000485515.5:n.357+122_357+123del
ENST00000491274.5:c.381+68_381+69del	ENSP00000480482.1:n.381+68_381+69del
NM_003000.2:c.423+68_423+69del , LRG_316t1:c.423+68_423+69del	NP_002991.2:n.423+68_423+69del
NM_003000.3:c.423+68_423+69del MANE Select	NP_002991.2:n.423+68_423+69del