Canonical Allele Identifier: CA416085919

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354286G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027791G>T , CM000663.2:g.17027791G>T	GRCh38
NC_000001.10:g.17354286G>T , CM000663.1:g.17354286G>T	GRCh37
NC_000001.9:g.17226873G>T	NCBI36
NG_012340.1:g.31380C>A , LRG_316:g.31380C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.327C>A	ENSP00000481376.2:p.Gly109=
ENST00000491274.6:c.456C>A	ENSP00000480482.2:p.Gly152=
ENST00000375499.8:c.498C>A MANE Select	ENSP00000364649.3:p.Gly166=
ENST00000375499.7:c.498C>A	ENSP00000364649.3:p.Gly166=
ENST00000463045.2:c.327C>A	ENSP00000481376.1:p.Gly109=
ENST00000475506.1:n.415C>A
ENST00000485515.5:n.432C>A
ENST00000491274.5:c.456C>A	ENSP00000480482.1:p.Gly152=
NM_003000.2:c.498C>A , LRG_316t1:c.498C>A	NP_002991.2:p.Gly166=
NM_003000.3:c.498C>A MANE Select	NP_002991.2:p.Gly166=