Canonical Allele Identifier: CA1156077991
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022653_17022657delinsTAGAG , CM000663.2:g.17022653_17022657delinsTAGAG GRCh38
NC_000001.10:g.17349148_17349152delinsTAGAG , CM000663.1:g.17349148_17349152delinsTAGAG GRCh37
NC_000001.9:g.17221735_17221739delinsTAGAG NCBI36
NG_012340.1:g.36514_36518delinsCTCTA , LRG_316:g.36514_36518delinsCTCTA

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.545_549delinsCTCTA ENSP00000481376.2:p.Ser182=
ENST00000491274.6:c.674_678delinsCTCTA ENSP00000480482.2:p.Ser225=
ENST00000375499.8:c.716_720delinsCTCTA MANE Select ENSP00000364649.3:p.Ser239=
ENST00000375499.7:c.716_720delinsCTCTA ENSP00000364649.3:p.Ser239=
ENST00000475049.5:n.141_145delinsCTCTA
ENST00000485092.5:n.380_384delinsCTCTA
ENST00000485515.5:n.650_654delinsCTCTA
NM_003000.2:c.716_720delinsCTCTA , LRG_316t1:c.716_720delinsCTCTA NP_002991.2:p.Ser239=
NM_003000.3:c.716_720delinsCTCTA MANE Select NP_002991.2:p.Ser239=