Canonical Allele Identifier: CA1156090669
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044724C= , CM000663.2:g.17044724C= GRCh38
NC_000001.10:g.17371219C= , CM000663.1:g.17371219C= GRCh37
NC_000001.9:g.17243806C= NCBI36
NG_012340.1:g.14447G= , LRG_316:g.14447G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.29+37G= ENSP00000481376.2:n.29+37G=
ENST00000491274.6:c.158+37G= ENSP00000480482.2:n.158+37G=
ENST00000375499.8:c.200+37G= MANE Select ENSP00000364649.3:n.200+37G=
ENST00000375499.7:c.200+37G= ENSP00000364649.3:n.200+37G=
ENST00000463045.2:c.29+37G= ENSP00000481376.1:n.29+37G=
ENST00000466613.2:n.212+37G=
ENST00000475506.1:n.117+37G=
ENST00000485515.5:n.188+37G=
ENST00000491274.5:c.158+37G= ENSP00000480482.1:n.158+37G=
NM_003000.2:c.200+37G= , LRG_316t1:c.200+37G= NP_002991.2:n.200+37G=
NM_003000.3:c.200+37G= MANE Select NP_002991.2:n.200+37G=