Canonical Allele Identifier: CA999084455

Gene: SDHB

Linked Data

• gnomAD v3: 1-17028291-TTA-T
• gnomAD v4: 1-17028291-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028293_17028294del , CM000663.2:g.17028293_17028294del	GRCh38
NC_000001.10:g.17354788_17354789del , CM000663.1:g.17354788_17354789del	GRCh37
NC_000001.9:g.17227375_17227376del	NCBI36
NG_012340.1:g.30878_30879del , LRG_316:g.30878_30879del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+307_252+308del	ENSP00000481376.2:n.252+307_252+308del
ENST00000491274.6:c.381+307_381+308del	ENSP00000480482.2:n.381+307_381+308del
ENST00000375499.8:c.423+307_423+308del MANE Select	ENSP00000364649.3:n.423+307_423+308del
ENST00000375499.7:c.423+307_423+308del	ENSP00000364649.3:n.423+307_423+308del
ENST00000463045.2:c.252+307_252+308del	ENSP00000481376.1:n.252+307_252+308del
ENST00000475506.1:n.340+307_340+308del
ENST00000485515.5:n.357+361_357+362del
ENST00000491274.5:c.381+307_381+308del	ENSP00000480482.1:n.381+307_381+308del
NM_003000.2:c.423+307_423+308del , LRG_316t1:c.423+307_423+308del	NP_002991.2:n.423+307_423+308del
NM_003000.3:c.423+307_423+308del MANE Select	NP_002991.2:n.423+307_423+308del