Canonical Allele Identifier: CA416088133

Gene: SDHB

Linked Data

• COSMIC: COSM3705250
• MyVariant Identifiers: chr1:g.17355224A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028729A>G , CM000663.2:g.17028729A>G	GRCh38
NC_000001.10:g.17355224A>G , CM000663.1:g.17355224A>G	GRCh37
NC_000001.9:g.17227811A>G	NCBI36
NG_012340.1:g.30442T>C , LRG_316:g.30442T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.123T>C	ENSP00000481376.2:p.Cys41=
ENST00000491274.6:c.252T>C	ENSP00000480482.2:p.Cys84=
ENST00000375499.8:c.294T>C MANE Select	ENSP00000364649.3:p.Cys98=
ENST00000375499.7:c.294T>C	ENSP00000364649.3:p.Cys98=
ENST00000463045.2:c.123T>C	ENSP00000481376.1:p.Cys41=
ENST00000475506.1:n.211T>C
ENST00000485515.5:n.282T>C
ENST00000491274.5:c.252T>C	ENSP00000480482.1:p.Cys84=
NM_003000.2:c.294T>C , LRG_316t1:c.294T>C	NP_002991.2:p.Cys98=
NM_003000.3:c.294T>C MANE Select	NP_002991.2:p.Cys98=