Canonical Allele Identifier: CA416089439

Gene: SDHB

Linked Data

• gnomAD v4: 1-17033115-G-T
• MyVariant Identifiers: chr1:g.17359610G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17033115G>T , CM000663.2:g.17033115G>T	GRCh38
NC_000001.10:g.17359610G>T , CM000663.1:g.17359610G>T	GRCh37
NC_000001.9:g.17232197G>T	NCBI36
NG_012340.1:g.26056C>A , LRG_316:g.26056C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.60C>A	ENSP00000481376.2:p.Ile20=
ENST00000491274.6:c.189C>A	ENSP00000480482.2:p.Ile63=
ENST00000375499.8:c.231C>A MANE Select	ENSP00000364649.3:p.Ile77=
ENST00000375499.7:c.231C>A	ENSP00000364649.3:p.Ile77=
ENST00000463045.2:c.60C>A	ENSP00000481376.1:p.Ile20=
ENST00000466613.2:n.243C>A
ENST00000475506.1:n.148C>A
ENST00000485515.5:n.219C>A
ENST00000491274.5:c.189C>A	ENSP00000480482.1:p.Ile63=
NM_003000.2:c.231C>A , LRG_316t1:c.231C>A	NP_002991.2:p.Ile77=
NM_003000.3:c.231C>A MANE Select	NP_002991.2:p.Ile77=