Canonical Allele Identifier: CA338275136

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355220A>C (hg19) ; chr1:g.17028725A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028725A>C , CM000663.2:g.17028725A>C	GRCh38
NC_000001.10:g.17355220A>C , CM000663.1:g.17355220A>C	GRCh37
NC_000001.9:g.17227807A>C	NCBI36
NG_012340.1:g.30446T>G , LRG_316:g.30446T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.127T>G	ENSP00000481376.2:p.Ser43Ala
ENST00000491274.6:c.256T>G	ENSP00000480482.2:p.Ser86Ala
ENST00000375499.8:c.298T>G MANE Select	ENSP00000364649.3:p.Ser100Ala
ENST00000375499.7:c.298T>G	ENSP00000364649.3:p.Ser100Ala
ENST00000463045.2:c.127T>G	ENSP00000481376.1:p.Ser43Ala
ENST00000475506.1:n.215T>G
ENST00000485515.5:n.286T>G
ENST00000491274.5:c.256T>G	ENSP00000480482.1:p.Ser86Ala
NM_003000.2:c.298T>G , LRG_316t1:c.298T>G	NP_002991.2:p.Ser100Ala
NM_003000.3:c.298T>G MANE Select	NP_002991.2:p.Ser100Ala