Canonical Allele Identifier: CA1156080088
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027605A= , CM000663.2:g.17027605A= GRCh38
NC_000001.10:g.17354100A= , CM000663.1:g.17354100A= GRCh37
NC_000001.9:g.17226687A= NCBI36
NG_012340.1:g.31566T= , LRG_316:g.31566T=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.369+144T= ENSP00000481376.2:n.369+144T=
ENST00000491274.6:c.498+144T= ENSP00000480482.2:n.498+144T=
ENST00000375499.8:c.540+144T= MANE Select ENSP00000364649.3:n.540+144T=
ENST00000375499.7:c.540+144T= ENSP00000364649.3:n.540+144T=
ENST00000485515.5:n.474+144T=
ENST00000491274.5:c.498+144T= ENSP00000480482.1:n.498+144T=
NM_003000.2:c.540+144T= , LRG_316t1:c.540+144T= NP_002991.2:n.540+144T=
NM_003000.3:c.540+144T= MANE Select NP_002991.2:n.540+144T=