Canonical Allele Identifier: CA1156080434
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028459A= , CM000663.2:g.17028459A= GRCh38
NC_000001.10:g.17354954A= , CM000663.1:g.17354954A= GRCh37
NC_000001.9:g.17227541A= NCBI36
NG_012340.1:g.30712T= , LRG_316:g.30712T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+141T= ENSP00000481376.2:n.252+141T=
ENST00000491274.6:c.381+141T= ENSP00000480482.2:n.381+141T=
ENST00000375499.8:c.423+141T= MANE Select ENSP00000364649.3:n.423+141T=
ENST00000375499.7:c.423+141T= ENSP00000364649.3:n.423+141T=
ENST00000463045.2:c.252+141T= ENSP00000481376.1:n.252+141T=
ENST00000475506.1:n.340+141T=
ENST00000485515.5:n.357+195T=
ENST00000491274.5:c.381+141T= ENSP00000480482.1:n.381+141T=
NM_003000.2:c.423+141T= , LRG_316t1:c.423+141T= NP_002991.2:n.423+141T=
NM_003000.3:c.423+141T= MANE Select NP_002991.2:n.423+141T=