Canonical Allele Identifier: CA1140335693
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044657T= , CM000663.2:g.17044657T= GRCh38
NC_000001.10:g.17371152T= , CM000663.1:g.17371152T= GRCh37
NC_000001.9:g.17243739T= NCBI36
NG_012340.1:g.14514A= , LRG_316:g.14514A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.29+104A= ENSP00000481376.2:n.29+104A=
ENST00000491274.6:c.158+104A= ENSP00000480482.2:n.158+104A=
ENST00000375499.8:c.200+104A= MANE Select ENSP00000364649.3:n.200+104A=
ENST00000375499.7:c.200+104A= ENSP00000364649.3:n.200+104A=
ENST00000463045.2:c.29+104A= ENSP00000481376.1:n.29+104A=
ENST00000466613.2:n.212+104A=
ENST00000475506.1:n.117+104A=
ENST00000485515.5:n.188+104A=
ENST00000491274.5:c.158+104A= ENSP00000480482.1:n.158+104A=
NM_003000.2:c.200+104A= , LRG_316t1:c.200+104A= NP_002991.2:n.200+104A=
NM_003000.3:c.200+104A= MANE Select NP_002991.2:n.200+104A=