Canonical Allele Identifier: CA338276583

Gene: SDHB

Linked Data

• ClinVar Variation Id: 640231
• ClinVar RCV Id: RCV000793209
• dbSNP Id: rs1570951427
• MyVariant Identifiers: chr1:g.17359610G>C (hg19) ; chr1:g.17033115G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17033115G>C , CM000663.2:g.17033115G>C	GRCh38
NC_000001.10:g.17359610G>C , CM000663.1:g.17359610G>C	GRCh37
NC_000001.9:g.17232197G>C	NCBI36
NG_012340.1:g.26056C>G , LRG_316:g.26056C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.60C>G	ENSP00000481376.2:p.Ile20Met
ENST00000491274.6:c.189C>G	ENSP00000480482.2:p.Ile63Met
ENST00000375499.8:c.231C>G MANE Select	ENSP00000364649.3:p.Ile77Met
ENST00000375499.7:c.231C>G	ENSP00000364649.3:p.Ile77Met
ENST00000463045.2:c.60C>G	ENSP00000481376.1:p.Ile20Met
ENST00000466613.2:n.243C>G
ENST00000475506.1:n.148C>G
ENST00000485515.5:n.219C>G
ENST00000491274.5:c.189C>G	ENSP00000480482.1:p.Ile63Met
NM_003000.2:c.231C>G , LRG_316t1:c.231C>G	NP_002991.2:p.Ile77Met
NM_003000.3:c.231C>G MANE Select	NP_002991.2:p.Ile77Met