Canonical Allele Identifier: CA2573130758

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1505305
• ClinVar RCV Id: RCV002048011
• dbSNP Id: rs2101541552

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044852_17044853delinsTT , CM000663.2:g.17044852_17044853delinsTT	GRCh38
NC_000001.10:g.17371347_17371348delinsTT , CM000663.1:g.17371347_17371348delinsTT	GRCh37
NC_000001.9:g.17243934_17243935delinsTT	NCBI36
NG_012340.1:g.14318_14319delinsAA , LRG_316:g.14318_14319delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-64_-63delinsAA	ENSP00000481376.2:n.-64_-63delinsAA
ENST00000491274.6:c.66_67delinsAA	ENSP00000480482.2:p.Pro23Thr
ENST00000375499.8:c.108_109delinsAA MANE Select	ENSP00000364649.3:p.Pro37Thr
ENST00000375499.7:c.108_109delinsAA	ENSP00000364649.3:p.Pro37Thr
ENST00000463045.2:c.-64_-63delinsAA	ENSP00000481376.1:n.-64_-63delinsAA
ENST00000466613.2:n.120_121delinsAA
ENST00000475506.1:n.25_26delinsAA
ENST00000485515.5:n.96_97delinsAA
ENST00000491274.5:c.66_67delinsAA	ENSP00000480482.1:p.Pro23Thr
NM_003000.2:c.108_109delinsAA , LRG_316t1:c.108_109delinsAA	NP_002991.2:p.Pro37Thr
NM_003000.3:c.108_109delinsAA MANE Select	NP_002991.2:p.Pro37Thr