Canonical Allele Identifier: CA1156077897
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022450A= , CM000663.2:g.17022450A= GRCh38
NC_000001.10:g.17348945A= , CM000663.1:g.17348945A= GRCh37
NC_000001.9:g.17221532A= NCBI36
NG_012340.1:g.36721T= , LRG_316:g.36721T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+158T= ENSP00000481376.2:n.594+158T=
ENST00000491274.6:c.723+158T= ENSP00000480482.2:n.723+158T=
ENST00000375499.8:c.765+158T= MANE Select ENSP00000364649.3:n.765+158T=
ENST00000375499.7:c.765+158T= ENSP00000364649.3:n.765+158T=
ENST00000475049.5:n.190+158T=
ENST00000485092.5:n.429+158T=
NM_003000.2:c.765+158T= , LRG_316t1:c.765+158T= NP_002991.2:n.765+158T=
NM_003000.3:c.765+158T= MANE Select NP_002991.2:n.765+158T=