Canonical Allele Identifier: CA416046865

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17371306G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044811G>A , CM000663.2:g.17044811G>A	GRCh38
NC_000001.10:g.17371306G>A , CM000663.1:g.17371306G>A	GRCh37
NC_000001.9:g.17243893G>A	NCBI36
NG_012340.1:g.14360C>T , LRG_316:g.14360C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-22C>T	ENSP00000481376.2:n.-22C>T
ENST00000491274.6:c.108C>T	ENSP00000480482.2:p.Asp36=
ENST00000375499.8:c.150C>T MANE Select	ENSP00000364649.3:p.Asp50=
ENST00000375499.7:c.150C>T	ENSP00000364649.3:p.Asp50=
ENST00000463045.2:c.-22C>T	ENSP00000481376.1:n.-22C>T
ENST00000466613.2:n.162C>T
ENST00000475506.1:n.67C>T
ENST00000485515.5:n.138C>T
ENST00000491274.5:c.108C>T	ENSP00000480482.1:p.Asp36=
NM_003000.2:c.150C>T , LRG_316t1:c.150C>T	NP_002991.2:p.Asp50=
NM_003000.3:c.150C>T MANE Select	NP_002991.2:p.Asp50=