Canonical Allele Identifier: CA416081807

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349130G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022635G>T , CM000663.2:g.17022635G>T	GRCh38
NC_000001.10:g.17349130G>T , CM000663.1:g.17349130G>T	GRCh37
NC_000001.9:g.17221717G>T	NCBI36
NG_012340.1:g.36536C>A , LRG_316:g.36536C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.567C>A	ENSP00000481376.2:p.Ile189=
ENST00000491274.6:c.696C>A	ENSP00000480482.2:p.Ile232=
ENST00000375499.8:c.738C>A MANE Select	ENSP00000364649.3:p.Ile246=
ENST00000375499.7:c.738C>A	ENSP00000364649.3:p.Ile246=
ENST00000475049.5:n.163C>A
ENST00000485092.5:n.402C>A
ENST00000485515.5:n.672C>A
NM_003000.2:c.738C>A , LRG_316t1:c.738C>A	NP_002991.2:p.Ile246=
NM_003000.3:c.738C>A MANE Select	NP_002991.2:p.Ile246=