Canonical Allele Identifier: CA1147213622
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028428G= , CM000663.2:g.17028428G= GRCh38
NC_000001.10:g.17354923G= , CM000663.1:g.17354923G= GRCh37
NC_000001.9:g.17227510G= NCBI36
NG_012340.1:g.30743C= , LRG_316:g.30743C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+172C= ENSP00000481376.2:n.252+172C=
ENST00000491274.6:c.381+172C= ENSP00000480482.2:n.381+172C=
ENST00000375499.8:c.423+172C= MANE Select ENSP00000364649.3:n.423+172C=
ENST00000375499.7:c.423+172C= ENSP00000364649.3:n.423+172C=
ENST00000463045.2:c.252+172C= ENSP00000481376.1:n.252+172C=
ENST00000475506.1:n.340+172C=
ENST00000485515.5:n.357+226C=
ENST00000491274.5:c.381+172C= ENSP00000480482.1:n.381+172C=
NM_003000.2:c.423+172C= , LRG_316t1:c.423+172C= NP_002991.2:n.423+172C=
NM_003000.3:c.423+172C= MANE Select NP_002991.2:n.423+172C=