Canonical Allele Identifier: CA2580060615

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2447651
• ClinVar RCV Id: RCV003167961 ; RCV003778956
• dbSNP Id: rs776039903

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022604G>C , CM000663.2:g.17022604G>C	GRCh38
NC_000001.10:g.17349099G>C , CM000663.1:g.17349099G>C	GRCh37
NC_000001.9:g.17221686G>C	NCBI36
NG_012340.1:g.36567C>G , LRG_316:g.36567C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+4C>G	ENSP00000481376.2:n.594+4C>G
ENST00000491274.6:c.723+4C>G	ENSP00000480482.2:n.723+4C>G
ENST00000375499.8:c.765+4C>G MANE Select	ENSP00000364649.3:n.765+4C>G
ENST00000375499.7:c.765+4C>G	ENSP00000364649.3:n.765+4C>G
ENST00000475049.5:n.190+4C>G
ENST00000485092.5:n.429+4C>G
NM_003000.2:c.765+4C>G , LRG_316t1:c.765+4C>G	NP_002991.2:n.765+4C>G
NM_003000.3:c.765+4C>G MANE Select	NP_002991.2:n.765+4C>G