Canonical Allele Identifier: CA416047192

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371369G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044874G>T , CM000663.2:g.17044874G>T	GRCh38
NC_000001.10:g.17371369G>T , CM000663.1:g.17371369G>T	GRCh37
NC_000001.9:g.17243956G>T	NCBI36
NG_012340.1:g.14297C>A , LRG_316:g.14297C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-85C>A	ENSP00000481376.2:n.-85C>A
ENST00000491274.6:c.45C>A	ENSP00000480482.2:p.Ala15=
ENST00000375499.8:c.87C>A MANE Select	ENSP00000364649.3:p.Ala29=
ENST00000375499.7:c.87C>A	ENSP00000364649.3:p.Ala29=
ENST00000463045.2:c.-85C>A	ENSP00000481376.1:n.-85C>A
ENST00000466613.2:n.99C>A
ENST00000475506.1:n.4C>A
ENST00000485515.5:n.75C>A
ENST00000491274.5:c.45C>A	ENSP00000480482.1:p.Ala15=
NM_003000.2:c.87C>A , LRG_316t1:c.87C>A	NP_002991.2:p.Ala29=
NM_003000.3:c.87C>A MANE Select	NP_002991.2:p.Ala29=