Canonical Allele Identifier: CA1156077956

Gene: SDHB

Linked Data

• dbSNP Id: rs2077967738

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022585T>A , CM000663.2:g.17022585T>A	GRCh38
NC_000001.10:g.17349080T>A , CM000663.1:g.17349080T>A	GRCh37
NC_000001.9:g.17221667T>A	NCBI36
NG_012340.1:g.36586A>T , LRG_316:g.36586A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+23A>T	ENSP00000481376.2:n.594+23A>T
ENST00000491274.6:c.723+23A>T	ENSP00000480482.2:n.723+23A>T
ENST00000375499.8:c.765+23A>T MANE Select	ENSP00000364649.3:n.765+23A>T
ENST00000375499.7:c.765+23A>T	ENSP00000364649.3:n.765+23A>T
ENST00000475049.5:n.190+23A>T
ENST00000485092.5:n.429+23A>T
NM_003000.2:c.765+23A>T , LRG_316t1:c.765+23A>T	NP_002991.2:n.765+23A>T
NM_003000.3:c.765+23A>T MANE Select	NP_002991.2:n.765+23A>T