Canonical Allele Identifier: CA338274968

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1907361
• ClinVar RCV Id: RCV002578179 ; RCV003164820
• MyVariant Identifiers: chr1:g.17355203G>C (hg19) ; chr1:g.17028708G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028708G>C , CM000663.2:g.17028708G>C	GRCh38
NC_000001.10:g.17355203G>C , CM000663.1:g.17355203G>C	GRCh37
NC_000001.9:g.17227790G>C	NCBI36
NG_012340.1:g.30463C>G , LRG_316:g.30463C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.144C>G	ENSP00000481376.2:p.Ile48Met
ENST00000491274.6:c.273C>G	ENSP00000480482.2:p.Ile91Met
ENST00000375499.8:c.315C>G MANE Select	ENSP00000364649.3:p.Ile105Met
ENST00000375499.7:c.315C>G	ENSP00000364649.3:p.Ile105Met
ENST00000463045.2:c.144C>G	ENSP00000481376.1:p.Ile48Met
ENST00000475506.1:n.232C>G
ENST00000485515.5:n.303C>G
ENST00000491274.5:c.273C>G	ENSP00000480482.1:p.Ile91Met
NM_003000.2:c.315C>G , LRG_316t1:c.315C>G	NP_002991.2:p.Ile105Met
NM_003000.3:c.315C>G MANE Select	NP_002991.2:p.Ile105Met