Canonical Allele Identifier: CA1156091031
Community Standard Title: NM_003000.3(SDHB):c.137G= (p.Arg46=)
Gene: SDHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17044824C= , CM000663.2:g.17044824C= GRCh38
NC_000001.10:g.17371319C= , CM000663.1:g.17371319C= GRCh37
NC_000001.9:g.17243906C= NCBI36
NG_012340.1:g.14347G= , LRG_316:g.14347G=

Transcript Alleles

HGVS Amino-acid Change
NM_003000.3:c.137G= MANE Select NP_002991.2:p.Arg46=
ENST00000375499.8:c.137G= MANE Select ENSP00000364649.3:p.Arg46=
NM_003000.2:c.137G= , LRG_316t1:c.137G= NP_002991.2:p.Arg46=
ENST00000375499.7:c.137G= ENSP00000364649.3:p.Arg46=
ENST00000463045.2:c.-35G= ENSP00000481376.1:n.-35G=
ENST00000463045.3:c.-35G= ENSP00000481376.2:n.-35G=
ENST00000466613.2:n.149G=
ENST00000475506.1:n.54G=
ENST00000485515.5:n.125G=
ENST00000491274.5:c.95G= ENSP00000480482.1:p.Arg32=
ENST00000491274.6:c.95G= ENSP00000480482.2:p.Arg32=