Canonical Allele Identifier: CA1156077785
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022175_17022176delinsGA , CM000663.2:g.17022175_17022176delinsGA GRCh38
NC_000001.10:g.17348670_17348671delinsGA , CM000663.1:g.17348670_17348671delinsGA GRCh37
NC_000001.9:g.17221257_17221258delinsGA NCBI36
NG_012340.1:g.36995_36996delinsTC , LRG_316:g.36995_36996delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+432_594+433delinsTC ENSP00000481376.2:n.594+432_594+433delinsTC
ENST00000491274.6:c.723+432_723+433delinsTC ENSP00000480482.2:n.723+432_723+433delinsTC
ENST00000375499.8:c.765+432_765+433delinsTC MANE Select ENSP00000364649.3:n.765+432_765+433delinsTC
ENST00000375499.7:c.765+432_765+433delinsTC ENSP00000364649.3:n.765+432_765+433delinsTC
ENST00000475049.5:n.190+432_190+433delinsTC
ENST00000485092.5:n.429+432_429+433delinsTC
NM_003000.2:c.765+432_765+433delinsTC , LRG_316t1:c.765+432_765+433delinsTC NP_002991.2:n.765+432_765+433delinsTC
NM_003000.3:c.765+432_765+433delinsTC MANE Select NP_002991.2:n.765+432_765+433delinsTC