Canonical Allele Identifier: CA416085981

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354295A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027800A>T , CM000663.2:g.17027800A>T	GRCh38
NC_000001.10:g.17354295A>T , CM000663.1:g.17354295A>T	GRCh37
NC_000001.9:g.17226882A>T	NCBI36
NG_012340.1:g.31371T>A , LRG_316:g.31371T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.318T>A	ENSP00000481376.2:p.Ser106=
ENST00000491274.6:c.447T>A	ENSP00000480482.2:p.Ser149=
ENST00000375499.8:c.489T>A MANE Select	ENSP00000364649.3:p.Ser163=
ENST00000375499.7:c.489T>A	ENSP00000364649.3:p.Ser163=
ENST00000463045.2:c.318T>A	ENSP00000481376.1:p.Ser106=
ENST00000475506.1:n.406T>A
ENST00000485515.5:n.423T>A
ENST00000491274.5:c.447T>A	ENSP00000480482.1:p.Ser149=
NM_003000.2:c.489T>A , LRG_316t1:c.489T>A	NP_002991.2:p.Ser163=
NM_003000.3:c.489T>A MANE Select	NP_002991.2:p.Ser163=