Canonical Allele Identifier: CA416085716

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354259T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027764T>C , CM000663.2:g.17027764T>C	GRCh38
NC_000001.10:g.17354259T>C , CM000663.1:g.17354259T>C	GRCh37
NC_000001.9:g.17226846T>C	NCBI36
NG_012340.1:g.31407A>G , LRG_316:g.31407A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.354A>G	ENSP00000481376.2:p.Glu118=
ENST00000491274.6:c.483A>G	ENSP00000480482.2:p.Glu161=
ENST00000375499.8:c.525A>G MANE Select	ENSP00000364649.3:p.Glu175=
ENST00000375499.7:c.525A>G	ENSP00000364649.3:p.Glu175=
ENST00000463045.2:c.354A>G	ENSP00000481376.1:p.Glu118=
ENST00000475506.1:n.442A>G
ENST00000485515.5:n.459A>G
ENST00000491274.5:c.483A>G	ENSP00000480482.1:p.Glu161=
NM_003000.2:c.525A>G , LRG_316t1:c.525A>G	NP_002991.2:p.Glu175=
NM_003000.3:c.525A>G MANE Select	NP_002991.2:p.Glu175=