Canonical Allele Identifier: CA416086088

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027815-C-T
• MyVariant Identifiers: chr1:g.17354310C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027815C>T , CM000663.2:g.17027815C>T	GRCh38
NC_000001.10:g.17354310C>T , CM000663.1:g.17354310C>T	GRCh37
NC_000001.9:g.17226897C>T	NCBI36
NG_012340.1:g.31356G>A , LRG_316:g.31356G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.303G>A	ENSP00000481376.2:p.Lys101=
ENST00000491274.6:c.432G>A	ENSP00000480482.2:p.Lys144=
ENST00000375499.8:c.474G>A MANE Select	ENSP00000364649.3:p.Lys158=
ENST00000375499.7:c.474G>A	ENSP00000364649.3:p.Lys158=
ENST00000463045.2:c.303G>A	ENSP00000481376.1:p.Lys101=
ENST00000475506.1:n.391G>A
ENST00000485515.5:n.408G>A
ENST00000491274.5:c.432G>A	ENSP00000480482.1:p.Lys144=
NM_003000.2:c.474G>A , LRG_316t1:c.474G>A	NP_002991.2:p.Lys158=
NM_003000.3:c.474G>A MANE Select	NP_002991.2:p.Lys158=