Canonical Allele Identifier: CA338270080

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349128A>C (hg19) ; chr1:g.17022633A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022633A>C , CM000663.2:g.17022633A>C	GRCh38
NC_000001.10:g.17349128A>C , CM000663.1:g.17349128A>C	GRCh37
NC_000001.9:g.17221715A>C	NCBI36
NG_012340.1:g.36538T>G , LRG_316:g.36538T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.569T>G	ENSP00000481376.2:p.Met190Arg
ENST00000491274.6:c.698T>G	ENSP00000480482.2:p.Met233Arg
ENST00000375499.8:c.740T>G MANE Select	ENSP00000364649.3:p.Met247Arg
ENST00000375499.7:c.740T>G	ENSP00000364649.3:p.Met247Arg
ENST00000475049.5:n.165T>G
ENST00000485092.5:n.404T>G
ENST00000485515.5:n.674T>G
NM_003000.2:c.740T>G , LRG_316t1:c.740T>G	NP_002991.2:p.Met247Arg
NM_003000.3:c.740T>G MANE Select	NP_002991.2:p.Met247Arg