Canonical Allele Identifier: CA1156101919
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17053953G= , CM000663.2:g.17053953G= GRCh38
NC_000001.10:g.17380448G= , CM000663.1:g.17380448G= GRCh37
NC_000001.9:g.17253035G= NCBI36
NG_012340.1:g.5218C= , LRG_316:g.5218C=

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.67C= MANE Select ENSP00000364649.3:p.Leu23=
ENST00000375499.7:c.67C= ENSP00000364649.3:p.Leu23=
ENST00000466613.2:n.79C=
ENST00000485515.5:n.55C=
NM_003000.2:c.67C= , LRG_316t1:c.67C= NP_002991.2:p.Leu23=
NM_003000.3:c.67C= MANE Select NP_002991.2:p.Leu23=