Canonical Allele Identifier: CA2695456696

Gene: SDHB

Linked Data

• dbSNP Id: rs2101522605

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028370_17028373del , CM000663.2:g.17028370_17028373del	GRCh38
NC_000001.10:g.17354865_17354868del , CM000663.1:g.17354865_17354868del	GRCh37
NC_000001.9:g.17227452_17227455del	NCBI36
NG_012340.1:g.30802_30805del , LRG_316:g.30802_30805del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+231_252+234del	ENSP00000481376.2:n.252+231_252+234del
ENST00000491274.6:c.381+231_381+234del	ENSP00000480482.2:n.381+231_381+234del
ENST00000375499.8:c.423+231_423+234del MANE Select	ENSP00000364649.3:n.423+231_423+234del
ENST00000375499.7:c.423+231_423+234del	ENSP00000364649.3:n.423+231_423+234del
ENST00000463045.2:c.252+231_252+234del	ENSP00000481376.1:n.252+231_252+234del
ENST00000475506.1:n.340+231_340+234del
ENST00000485515.5:n.357+285_357+288del
ENST00000491274.5:c.381+231_381+234del	ENSP00000480482.1:n.381+231_381+234del
NM_003000.2:c.423+231_423+234del , LRG_316t1:c.423+231_423+234del	NP_002991.2:n.423+231_423+234del
NM_003000.3:c.423+231_423+234del MANE Select	NP_002991.2:n.423+231_423+234del