Canonical Allele Identifier: CA338271060

Gene: SDHB

Linked Data

• gnomAD v4: 1-17024014-A-T
• MyVariant Identifiers: chr1:g.17350509A>T (hg19) ; chr1:g.17024014A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17024014A>T , CM000663.2:g.17024014A>T	GRCh38
NC_000001.10:g.17350509A>T , CM000663.1:g.17350509A>T	GRCh37
NC_000001.9:g.17223096A>T	NCBI36
NG_012340.1:g.35157T>A , LRG_316:g.35157T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.430T>A	ENSP00000481376.2:p.Trp144Arg
ENST00000491274.6:c.559T>A	ENSP00000480482.2:p.Trp187Arg
ENST00000375499.8:c.601T>A MANE Select	ENSP00000364649.3:p.Trp201Arg
ENST00000375499.7:c.601T>A	ENSP00000364649.3:p.Trp201Arg
ENST00000485515.5:n.535T>A
ENST00000491274.5:c.559T>A	ENSP00000480482.1:p.Trp187Arg
NM_003000.2:c.601T>A , LRG_316t1:c.601T>A	NP_002991.2:p.Trp201Arg
NM_003000.3:c.601T>A MANE Select	NP_002991.2:p.Trp201Arg