Canonical Allele Identifier: CA338269997
Gene: SDHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022618G>T , CM000663.2:g.17022618G>T GRCh38
NC_000001.10:g.17349113G>T , CM000663.1:g.17349113G>T GRCh37
NC_000001.9:g.17221700G>T NCBI36
NG_012340.1:g.36553C>A , LRG_316:g.36553C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.584C>A ENSP00000481376.2:p.Thr195Asn
ENST00000491274.6:c.713C>A ENSP00000480482.2:p.Thr238Asn
ENST00000375499.8:c.755C>A MANE Select ENSP00000364649.3:p.Thr252Asn
ENST00000375499.7:c.755C>A ENSP00000364649.3:p.Thr252Asn
ENST00000475049.5:n.180C>A
ENST00000485092.5:n.419C>A
ENST00000485515.5:n.689C>A
NM_003000.2:c.755C>A , LRG_316t1:c.755C>A NP_002991.2:p.Thr252Asn
NM_003000.3:c.755C>A MANE Select NP_002991.2:p.Thr252Asn