Canonical Allele Identifier: CA416047164

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371363T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044868T>G , CM000663.2:g.17044868T>G	GRCh38
NC_000001.10:g.17371363T>G , CM000663.1:g.17371363T>G	GRCh37
NC_000001.9:g.17243950T>G	NCBI36
NG_012340.1:g.14303A>C , LRG_316:g.14303A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-79A>C	ENSP00000481376.2:n.-79A>C
ENST00000491274.6:c.51A>C	ENSP00000480482.2:p.Thr17=
ENST00000375499.8:c.93A>C MANE Select	ENSP00000364649.3:p.Thr31=
ENST00000375499.7:c.93A>C	ENSP00000364649.3:p.Thr31=
ENST00000463045.2:c.-79A>C	ENSP00000481376.1:n.-79A>C
ENST00000466613.2:n.105A>C
ENST00000475506.1:n.10A>C
ENST00000485515.5:n.81A>C
ENST00000491274.5:c.51A>C	ENSP00000480482.1:p.Thr17=
NM_003000.2:c.93A>C , LRG_316t1:c.93A>C	NP_002991.2:p.Thr31=
NM_003000.3:c.93A>C MANE Select	NP_002991.2:p.Thr31=