Canonical Allele Identifier: CA645509071

Gene: SDHB

Linked Data

• ClinVar Variation Id: 438419
• ClinVar RCV Id: RCV000505289 ; RCV001215683 ; RCV002438228
• dbSNP Id: rs1553177772
• MyVariant Identifiers: chr1:g.17355234G>C (hg19) ; chr1:g.17028739G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028739G>C , CM000663.2:g.17028739G>C	GRCh38
NC_000001.10:g.17355234G>C , CM000663.1:g.17355234G>C	GRCh37
NC_000001.9:g.17227821G>C	NCBI36
NG_012340.1:g.30432C>G , LRG_316:g.30432C>G

Transcript Alleles

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