Canonical Allele Identifier: CA416088118

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355221G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028726G>A , CM000663.2:g.17028726G>A	GRCh38
NC_000001.10:g.17355221G>A , CM000663.1:g.17355221G>A	GRCh37
NC_000001.9:g.17227808G>A	NCBI36
NG_012340.1:g.30445C>T , LRG_316:g.30445C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.126C>T	ENSP00000481376.2:p.Gly42=
ENST00000491274.6:c.255C>T	ENSP00000480482.2:p.Gly85=
ENST00000375499.8:c.297C>T MANE Select	ENSP00000364649.3:p.Gly99=
ENST00000375499.7:c.297C>T	ENSP00000364649.3:p.Gly99=
ENST00000463045.2:c.126C>T	ENSP00000481376.1:p.Gly42=
ENST00000475506.1:n.214C>T
ENST00000485515.5:n.285C>T
ENST00000491274.5:c.255C>T	ENSP00000480482.1:p.Gly85=
NM_003000.2:c.297C>T , LRG_316t1:c.297C>T	NP_002991.2:p.Gly99=
NM_003000.3:c.297C>T MANE Select	NP_002991.2:p.Gly99=