Canonical Allele Identifier: CA1156077900
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022453A= , CM000663.2:g.17022453A= GRCh38
NC_000001.10:g.17348948A= , CM000663.1:g.17348948A= GRCh37
NC_000001.9:g.17221535A= NCBI36
NG_012340.1:g.36718T= , LRG_316:g.36718T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+155T= ENSP00000481376.2:n.594+155T=
ENST00000491274.6:c.723+155T= ENSP00000480482.2:n.723+155T=
ENST00000375499.8:c.765+155T= MANE Select ENSP00000364649.3:n.765+155T=
ENST00000375499.7:c.765+155T= ENSP00000364649.3:n.765+155T=
ENST00000475049.5:n.190+155T=
ENST00000485092.5:n.429+155T=
NM_003000.2:c.765+155T= , LRG_316t1:c.765+155T= NP_002991.2:n.765+155T=
NM_003000.3:c.765+155T= MANE Select NP_002991.2:n.765+155T=