Canonical Allele Identifier: CA416047102

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1779668
• ClinVar RCV Id: RCV002407635
• MyVariant Identifiers: chr1:g.17371351T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044856T>G , CM000663.2:g.17044856T>G	GRCh38
NC_000001.10:g.17371351T>G , CM000663.1:g.17371351T>G	GRCh37
NC_000001.9:g.17243938T>G	NCBI36
NG_012340.1:g.14315A>C , LRG_316:g.14315A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-67A>C	ENSP00000481376.2:n.-67A>C
ENST00000491274.6:c.63A>C	ENSP00000480482.2:p.Thr21=
ENST00000375499.8:c.105A>C MANE Select	ENSP00000364649.3:p.Thr35=
ENST00000375499.7:c.105A>C	ENSP00000364649.3:p.Thr35=
ENST00000463045.2:c.-67A>C	ENSP00000481376.1:n.-67A>C
ENST00000466613.2:n.117A>C
ENST00000475506.1:n.22A>C
ENST00000485515.5:n.93A>C
ENST00000491274.5:c.63A>C	ENSP00000480482.1:p.Thr21=
NM_003000.2:c.105A>C , LRG_316t1:c.105A>C	NP_002991.2:p.Thr35=
NM_003000.3:c.105A>C MANE Select	NP_002991.2:p.Thr35=