Canonical Allele Identifier: CA2695449110
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2101514068

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022738_17022739insGAACTGCAGGCCCCAGATATTTGTCT , CM000663.2:g.17022738_17022739insGAACTGCAGGCCCCAGATATTTGTCT GRCh38
NC_000001.10:g.17349233_17349234insGAACTGCAGGCCCCAGATATTTGTCT , CM000663.1:g.17349233_17349234insGAACTGCAGGCCCCAGATATTTGTCT GRCh37
NC_000001.9:g.17221820_17221821insGAACTGCAGGCCCCAGATATTTGTCT NCBI36
NG_012340.1:g.36432_36433insAGACAAATATCTGGGGCCTGCAGTTC , LRG_316:g.36432_36433insAGACAAATATCTGGGGCCTGCAGTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.472-9_472-8insAGACAAATATCTGGGGCCTGCAGTTC ENSP00000481376.2:n.472-9_472-8insAGACAAATATCTGGGGCCTGCAGTTC
ENST00000491274.6:c.601-9_601-8insAGACAAATATCTGGGGCCTGCAGTTC ENSP00000480482.2:n.601-9_601-8insAGACAAATATCTGGGGCCTGCAGTTC
ENST00000375499.8:c.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC MANE Select ENSP00000364649.3:n.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC
ENST00000375499.7:c.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC ENSP00000364649.3:n.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC
ENST00000475049.5:n.68-9_68-8insAGACAAATATCTGGGGCCTGCAGTTC
ENST00000485092.5:n.298_299insAGACAAATATCTGGGGCCTGCAGTTC
ENST00000485515.5:n.577-9_577-8insAGACAAATATCTGGGGCCTGCAGTTC
NM_003000.2:c.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC , LRG_316t1:c.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC NP_002991.2:n.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC
NM_003000.3:c.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC MANE Select NP_002991.2:n.643-9_643-8insAGACAAATATCTGGGGCCTGCAGTTC