Canonical Allele Identifier: CA1156080449
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028509C= , CM000663.2:g.17028509C= GRCh38
NC_000001.10:g.17355004C= , CM000663.1:g.17355004C= GRCh37
NC_000001.9:g.17227591C= NCBI36
NG_012340.1:g.30662G= , LRG_316:g.30662G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.252+91G= ENSP00000481376.2:n.252+91G=
ENST00000491274.6:c.381+91G= ENSP00000480482.2:n.381+91G=
ENST00000375499.8:c.423+91G= MANE Select ENSP00000364649.3:n.423+91G=
ENST00000375499.7:c.423+91G= ENSP00000364649.3:n.423+91G=
ENST00000463045.2:c.252+91G= ENSP00000481376.1:n.252+91G=
ENST00000475506.1:n.340+91G=
ENST00000485515.5:n.357+145G=
ENST00000491274.5:c.381+91G= ENSP00000480482.1:n.381+91G=
NM_003000.2:c.423+91G= , LRG_316t1:c.423+91G= NP_002991.2:n.423+91G=
NM_003000.3:c.423+91G= MANE Select NP_002991.2:n.423+91G=