Canonical Allele Identifier: CA1156077904
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022458_17022459delinsCT , CM000663.2:g.17022458_17022459delinsCT GRCh38
NC_000001.10:g.17348953_17348954delinsCT , CM000663.1:g.17348953_17348954delinsCT GRCh37
NC_000001.9:g.17221540_17221541delinsCT NCBI36
NG_012340.1:g.36712_36713delinsAG , LRG_316:g.36712_36713delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+149_594+150delinsAG ENSP00000481376.2:n.594+149_594+150delinsAG
ENST00000491274.6:c.723+149_723+150delinsAG ENSP00000480482.2:n.723+149_723+150delinsAG
ENST00000375499.8:c.765+149_765+150delinsAG MANE Select ENSP00000364649.3:n.765+149_765+150delinsAG
ENST00000375499.7:c.765+149_765+150delinsAG ENSP00000364649.3:n.765+149_765+150delinsAG
ENST00000475049.5:n.190+149_190+150delinsAG
ENST00000485092.5:n.429+149_429+150delinsAG
NM_003000.2:c.765+149_765+150delinsAG , LRG_316t1:c.765+149_765+150delinsAG NP_002991.2:n.765+149_765+150delinsAG
NM_003000.3:c.765+149_765+150delinsAG MANE Select NP_002991.2:n.765+149_765+150delinsAG