Canonical Allele Identifier: CA416085942

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027794-T-C
• MyVariant Identifiers: chr1:g.17354289T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027794T>C , CM000663.2:g.17027794T>C	GRCh38
NC_000001.10:g.17354289T>C , CM000663.1:g.17354289T>C	GRCh37
NC_000001.9:g.17226876T>C	NCBI36
NG_012340.1:g.31377A>G , LRG_316:g.31377A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.324A>G	ENSP00000481376.2:p.Glu108=
ENST00000491274.6:c.453A>G	ENSP00000480482.2:p.Glu151=
ENST00000375499.8:c.495A>G MANE Select	ENSP00000364649.3:p.Glu165=
ENST00000375499.7:c.495A>G	ENSP00000364649.3:p.Glu165=
ENST00000463045.2:c.324A>G	ENSP00000481376.1:p.Glu108=
ENST00000475506.1:n.412A>G
ENST00000485515.5:n.429A>G
ENST00000491274.5:c.453A>G	ENSP00000480482.1:p.Glu151=
NM_003000.2:c.495A>G , LRG_316t1:c.495A>G	NP_002991.2:p.Glu165=
NM_003000.3:c.495A>G MANE Select	NP_002991.2:p.Glu165=