Canonical Allele Identifier: CA1156102291
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17054019T= , CM000663.2:g.17054019T= GRCh38
NC_000001.10:g.17380514T= , CM000663.1:g.17380514T= GRCh37
NC_000001.9:g.17253101T= NCBI36
NG_012340.1:g.5152A= , LRG_316:g.5152A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375499.8:c.1A= MANE Select ENSP00000364649.3:p.Met1=
ENST00000375499.7:c.1A= ENSP00000364649.3:p.Met1=
ENST00000466613.2:n.13A=
NM_003000.2:c.1A= , LRG_316t1:c.1A= NP_002991.2:p.Met1=
NM_003000.3:c.1A= MANE Select NP_002991.2:p.Met1=