Canonical Allele Identifier: CA338228108

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1952317
• ClinVar RCV Id: RCV002695264
• gnomAD v4: 1-17044827-T-C
• MyVariant Identifiers: chr1:g.17371322T>C (hg19) ; chr1:g.17044827T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044827T>C , CM000663.2:g.17044827T>C	GRCh38
NC_000001.10:g.17371322T>C , CM000663.1:g.17371322T>C	GRCh37
NC_000001.9:g.17243909T>C	NCBI36
NG_012340.1:g.14344A>G , LRG_316:g.14344A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-38A>G	ENSP00000481376.2:n.-38A>G
ENST00000491274.6:c.92A>G	ENSP00000480482.2:p.Tyr31Cys
ENST00000375499.8:c.134A>G MANE Select	ENSP00000364649.3:p.Tyr45Cys
ENST00000375499.7:c.134A>G	ENSP00000364649.3:p.Tyr45Cys
ENST00000463045.2:c.-38A>G	ENSP00000481376.1:n.-38A>G
ENST00000466613.2:n.146A>G
ENST00000475506.1:n.51A>G
ENST00000485515.5:n.122A>G
ENST00000491274.5:c.92A>G	ENSP00000480482.1:p.Tyr31Cys
NM_003000.2:c.134A>G , LRG_316t1:c.134A>G	NP_002991.2:p.Tyr45Cys
NM_003000.3:c.134A>G MANE Select	NP_002991.2:p.Tyr45Cys