Canonical Allele Identifier: CA18610404

Gene: SDHB

Linked Data

• ClinVar Variation Id: 856938
• ClinVar RCV Id: RCV001062511 ; RCV004000127
• dbSNP Id: rs770733541
• MyVariant Identifiers: chr1:g.17371390T>G (hg19) ; chr1:g.17044895T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044895T>G , CM000663.2:g.17044895T>G	GRCh38
NC_000001.10:g.17371390T>G , CM000663.1:g.17371390T>G	GRCh37
NC_000001.9:g.17243977T>G	NCBI36
NG_012340.1:g.14276A>C , LRG_316:g.14276A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-99-7A>C	ENSP00000481376.2:n.-99-7A>C
ENST00000491274.6:c.31-7A>C	ENSP00000480482.2:n.31-7A>C
ENST00000375499.8:c.73-7A>C MANE Select	ENSP00000364649.3:n.73-7A>C
ENST00000375499.7:c.73-7A>C	ENSP00000364649.3:n.73-7A>C
ENST00000463045.2:c.-99-7A>C	ENSP00000481376.1:n.-99-7A>C
ENST00000466613.2:n.85-7A>C
ENST00000485515.5:n.61-7A>C
ENST00000491274.5:c.31-7A>C	ENSP00000480482.1:n.31-7A>C
NM_003000.2:c.73-7A>C , LRG_316t1:c.73-7A>C	NP_002991.2:n.73-7A>C
NM_003000.3:c.73-7A>C MANE Select	NP_002991.2:n.73-7A>C