Canonical Allele Identifier: CA338228338

Gene: SDHB

Linked Data

• ClinVar Variation Id: 664395
• ClinVar RCV Id: RCV000822484
• dbSNP Id: rs1570958135
• MyVariant Identifiers: chr1:g.17371361G>A (hg19) ; chr1:g.17044866G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044866G>A , CM000663.2:g.17044866G>A	GRCh38
NC_000001.10:g.17371361G>A , CM000663.1:g.17371361G>A	GRCh37
NC_000001.9:g.17243948G>A	NCBI36
NG_012340.1:g.14305C>T , LRG_316:g.14305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-77C>T	ENSP00000481376.2:n.-77C>T
ENST00000491274.6:c.53C>T	ENSP00000480482.2:p.Ala18Val
ENST00000375499.8:c.95C>T MANE Select	ENSP00000364649.3:p.Ala32Val
ENST00000375499.7:c.95C>T	ENSP00000364649.3:p.Ala32Val
ENST00000463045.2:c.-77C>T	ENSP00000481376.1:n.-77C>T
ENST00000466613.2:n.107C>T
ENST00000475506.1:n.12C>T
ENST00000485515.5:n.83C>T
ENST00000491274.5:c.53C>T	ENSP00000480482.1:p.Ala18Val
NM_003000.2:c.95C>T , LRG_316t1:c.95C>T	NP_002991.2:p.Ala32Val
NM_003000.3:c.95C>T MANE Select	NP_002991.2:p.Ala32Val