Canonical Allele Identifier: CA2695197979

Gene: SDHB

Linked Data

• ClinVar Variation Id: 2678647
• ClinVar RCV Id: RCV003472643

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028742A>G , CM000663.2:g.17028742A>G	GRCh38
NC_000001.10:g.17355237A>G , CM000663.1:g.17355237A>G	GRCh37
NC_000001.9:g.17227824A>G	NCBI36
NG_012340.1:g.30429T>C , LRG_316:g.30429T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.116-6T>C	ENSP00000481376.2:n.116-6T>C
ENST00000491274.6:c.245-6T>C	ENSP00000480482.2:n.245-6T>C
ENST00000375499.8:c.287-6T>C MANE Select	ENSP00000364649.3:n.287-6T>C
ENST00000375499.7:c.287-6T>C	ENSP00000364649.3:n.287-6T>C
ENST00000463045.2:c.116-6T>C	ENSP00000481376.1:n.116-6T>C
ENST00000475506.1:n.204-6T>C
ENST00000485515.5:n.275-6T>C
ENST00000491274.5:c.245-6T>C	ENSP00000480482.1:n.245-6T>C
NM_003000.2:c.287-6T>C , LRG_316t1:c.287-6T>C	NP_002991.2:n.287-6T>C
NM_003000.3:c.287-6T>C MANE Select	NP_002991.2:n.287-6T>C