Canonical Allele Identifier: CA416082031

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349175C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022680C>A , CM000663.2:g.17022680C>A	GRCh38
NC_000001.10:g.17349175C>A , CM000663.1:g.17349175C>A	GRCh37
NC_000001.9:g.17221762C>A	NCBI36
NG_012340.1:g.36491G>T , LRG_316:g.36491G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.522G>T	ENSP00000481376.2:p.Leu174=
ENST00000491274.6:c.651G>T	ENSP00000480482.2:p.Leu217=
ENST00000375499.8:c.693G>T MANE Select	ENSP00000364649.3:p.Leu231=
ENST00000375499.7:c.693G>T	ENSP00000364649.3:p.Leu231=
ENST00000475049.5:n.118G>T
ENST00000485092.5:n.357G>T
ENST00000485515.5:n.627G>T
NM_003000.2:c.693G>T , LRG_316t1:c.693G>T	NP_002991.2:p.Leu231=
NM_003000.3:c.693G>T MANE Select	NP_002991.2:p.Leu231=