Canonical Allele Identifier: CA338275155

Gene: SDHB

Linked Data

• dbSNP Id: rs878854576
• MyVariant Identifiers: chr1:g.17355222C>A (hg19) ; chr1:g.17028727C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028727C>A , CM000663.2:g.17028727C>A	GRCh38
NC_000001.10:g.17355222C>A , CM000663.1:g.17355222C>A	GRCh37
NC_000001.9:g.17227809C>A	NCBI36
NG_012340.1:g.30444G>T , LRG_316:g.30444G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.125G>T	ENSP00000481376.2:p.Gly42Val
ENST00000491274.6:c.254G>T	ENSP00000480482.2:p.Gly85Val
ENST00000375499.8:c.296G>T MANE Select	ENSP00000364649.3:p.Gly99Val
ENST00000375499.7:c.296G>T	ENSP00000364649.3:p.Gly99Val
ENST00000463045.2:c.125G>T	ENSP00000481376.1:p.Gly42Val
ENST00000475506.1:n.213G>T
ENST00000485515.5:n.284G>T
ENST00000491274.5:c.254G>T	ENSP00000480482.1:p.Gly85Val
NM_003000.2:c.296G>T , LRG_316t1:c.296G>T	NP_002991.2:p.Gly99Val
NM_003000.3:c.296G>T MANE Select	NP_002991.2:p.Gly99Val