Canonical Allele Identifier: CA1146226690
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028625A= , CM000663.2:g.17028625A= GRCh38
NC_000001.10:g.17355120A= , CM000663.1:g.17355120A= GRCh37
NC_000001.9:g.17227707A= NCBI36
NG_012340.1:g.30546T= , LRG_316:g.30546T=

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.227T= ENSP00000481376.2:p.Met76=
ENST00000491274.6:c.356T= ENSP00000480482.2:p.Met119=
ENST00000375499.8:c.398T= MANE Select ENSP00000364649.3:p.Met133=
ENST00000375499.7:c.398T= ENSP00000364649.3:p.Met133=
ENST00000463045.2:c.227T= ENSP00000481376.1:p.Met76=
ENST00000475506.1:n.315T=
ENST00000485515.5:n.357+29T=
ENST00000491274.5:c.356T= ENSP00000480482.1:p.Met119=
NM_003000.2:c.398T= , LRG_316t1:c.398T= NP_002991.2:p.Met133=
NM_003000.3:c.398T= MANE Select NP_002991.2:p.Met133=