Canonical Allele Identifier: CA416082169

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349220A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022725A>G , CM000663.2:g.17022725A>G	GRCh38
NC_000001.10:g.17349220A>G , CM000663.1:g.17349220A>G	GRCh37
NC_000001.9:g.17221807A>G	NCBI36
NG_012340.1:g.36446T>C , LRG_316:g.36446T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.477T>C	ENSP00000481376.2:p.Tyr159=
ENST00000491274.6:c.606T>C	ENSP00000480482.2:p.Tyr202=
ENST00000375499.8:c.648T>C MANE Select	ENSP00000364649.3:p.Tyr216=
ENST00000375499.7:c.648T>C	ENSP00000364649.3:p.Tyr216=
ENST00000475049.5:n.73T>C
ENST00000485092.5:n.312T>C
ENST00000485515.5:n.582T>C
NM_003000.2:c.648T>C , LRG_316t1:c.648T>C	NP_002991.2:p.Tyr216=
NM_003000.3:c.648T>C MANE Select	NP_002991.2:p.Tyr216=