Canonical Allele Identifier: CA338270000

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349114T>C (hg19) ; chr1:g.17022619T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022619T>C , CM000663.2:g.17022619T>C	GRCh38
NC_000001.10:g.17349114T>C , CM000663.1:g.17349114T>C	GRCh37
NC_000001.9:g.17221701T>C	NCBI36
NG_012340.1:g.36552A>G , LRG_316:g.36552A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.583A>G	ENSP00000481376.2:p.Thr195Ala
ENST00000491274.6:c.712A>G	ENSP00000480482.2:p.Thr238Ala
ENST00000375499.8:c.754A>G MANE Select	ENSP00000364649.3:p.Thr252Ala
ENST00000375499.7:c.754A>G	ENSP00000364649.3:p.Thr252Ala
ENST00000475049.5:n.179A>G
ENST00000485092.5:n.418A>G
ENST00000485515.5:n.688A>G
NM_003000.2:c.754A>G , LRG_316t1:c.754A>G	NP_002991.2:p.Thr252Ala
NM_003000.3:c.754A>G MANE Select	NP_002991.2:p.Thr252Ala