Canonical Allele Identifier: CA338228456

Gene: SDHB

Linked Data

• dbSNP Id: rs1131691055
• MyVariant Identifiers: chr1:g.17371384C>G (hg19) ; chr1:g.17044889C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044889C>G , CM000663.2:g.17044889C>G	GRCh38
NC_000001.10:g.17371384C>G , CM000663.1:g.17371384C>G	GRCh37
NC_000001.9:g.17243971C>G	NCBI36
NG_012340.1:g.14282G>C , LRG_316:g.14282G>C

Transcript Alleles

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