Canonical Allele Identifier: CA416082086

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349187T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022692T>A , CM000663.2:g.17022692T>A	GRCh38
NC_000001.10:g.17349187T>A , CM000663.1:g.17349187T>A	GRCh37
NC_000001.9:g.17221774T>A	NCBI36
NG_012340.1:g.36479A>T , LRG_316:g.36479A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.510A>T	ENSP00000481376.2:p.Thr170=
ENST00000491274.6:c.639A>T	ENSP00000480482.2:p.Thr213=
ENST00000375499.8:c.681A>T MANE Select	ENSP00000364649.3:p.Thr227=
ENST00000375499.7:c.681A>T	ENSP00000364649.3:p.Thr227=
ENST00000475049.5:n.106A>T
ENST00000485092.5:n.345A>T
ENST00000485515.5:n.615A>T
NM_003000.2:c.681A>T , LRG_316t1:c.681A>T	NP_002991.2:p.Thr227=
NM_003000.3:c.681A>T MANE Select	NP_002991.2:p.Thr227=