Canonical Allele Identifier: CA1156077832
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022301_17022305delinsGCTTT , CM000663.2:g.17022301_17022305delinsGCTTT GRCh38
NC_000001.10:g.17348796_17348800delinsGCTTT , CM000663.1:g.17348796_17348800delinsGCTTT GRCh37
NC_000001.9:g.17221383_17221387delinsGCTTT NCBI36
NG_012340.1:g.36866_36870delinsAAAGC , LRG_316:g.36866_36870delinsAAAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+303_594+307delinsAAAGC ENSP00000481376.2:n.594+303_594+307delinsAAAGC
ENST00000491274.6:c.723+303_723+307delinsAAAGC ENSP00000480482.2:n.723+303_723+307delinsAAAGC
ENST00000375499.8:c.765+303_765+307delinsAAAGC MANE Select ENSP00000364649.3:n.765+303_765+307delinsAAAGC
ENST00000375499.7:c.765+303_765+307delinsAAAGC ENSP00000364649.3:n.765+303_765+307delinsAAAGC
ENST00000475049.5:n.190+303_190+307delinsAAAGC
ENST00000485092.5:n.429+303_429+307delinsAAAGC
NM_003000.2:c.765+303_765+307delinsAAAGC , LRG_316t1:c.765+303_765+307delinsAAAGC NP_002991.2:n.765+303_765+307delinsAAAGC
NM_003000.3:c.765+303_765+307delinsAAAGC MANE Select NP_002991.2:n.765+303_765+307delinsAAAGC