Canonical Allele Identifier: CA338271050

Gene: SDHB

Linked Data

• gnomAD v4: 1-17024013-C-A
• MyVariant Identifiers: chr1:g.17350508C>A (hg19) ; chr1:g.17024013C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17024013C>A , CM000663.2:g.17024013C>A	GRCh38
NC_000001.10:g.17350508C>A , CM000663.1:g.17350508C>A	GRCh37
NC_000001.9:g.17223095C>A	NCBI36
NG_012340.1:g.35158G>T , LRG_316:g.35158G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.431G>T	ENSP00000481376.2:p.Trp144Leu
ENST00000491274.6:c.560G>T	ENSP00000480482.2:p.Trp187Leu
ENST00000375499.8:c.602G>T MANE Select	ENSP00000364649.3:p.Trp201Leu
ENST00000375499.7:c.602G>T	ENSP00000364649.3:p.Trp201Leu
ENST00000485515.5:n.536G>T
ENST00000491274.5:c.560G>T	ENSP00000480482.1:p.Trp187Leu
NM_003000.2:c.602G>T , LRG_316t1:c.602G>T	NP_002991.2:p.Trp201Leu
NM_003000.3:c.602G>T MANE Select	NP_002991.2:p.Trp201Leu