Canonical Allele Identifier: CA9735158

Gene: IDH3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2660045G>A , CM000682.2:g.2660045G>A	GRCh38
NC_000020.10:g.2640691G>A , CM000682.1:g.2640691G>A	GRCh37
NC_000020.9:g.2588691G>A	NCBI36
NG_012149.1:g.9153C>T
NG_032136.1:g.12514G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006899.5:c.900C>T MANE Select	NP_008830.2:p.Tyr300=
ENST00000380843.9:c.900C>T MANE Select	ENSP00000370223.4:p.Tyr300=
NM_001258384.1:c.900C>T	NP_001245313.1:p.Tyr300=
NM_001258384.2:c.900C>T	NP_001245313.1:p.Tyr300=
NM_001258384.3:c.900C>T	NP_001245313.1:p.Tyr300=
NM_001330763.1:c.900C>T	NP_001317692.1:p.Tyr300=
NM_001330763.2:c.900C>T	NP_001317692.1:p.Tyr300=
NM_006899.3:c.900C>T	NP_008830.2:p.Tyr300=
NM_006899.4:c.900C>T	NP_008830.2:p.Tyr300=
NM_174855.2:c.900C>T	NP_777280.1:p.Tyr300=
NM_174855.3:c.900C>T	NP_777280.1:p.Tyr300=
NM_174855.4:c.900C>T	NP_777280.1:p.Tyr300=
NR_136344.1:n.935C>T
NR_136344.2:n.928C>T
ENST00000380843.8:c.900C>T	ENSP00000370223.4:p.Tyr300=
ENST00000380851.9:c.900C>T	ENSP00000370232.5:p.Tyr300=
ENST00000466494.6:c.178C>T
ENST00000474315.5:c.900C>T	ENSP00000482773.1:p.Tyr300=
ENST00000477689.2:c.156+23C>T
ENST00000479376.1:n.423C>T
ENST00000488299.5:n.1006C>T
ENST00000492240.5:n.229C>T
ENST00000613370.1:c.900C>T	ENSP00000484922.1:p.Tyr300=
XM_005260716.1:c.900C>T	XP_005260773.1:p.Tyr300=
XR_001754265.1:n.905+23C>T
XR_001754266.1:n.905+23C>T
XR_001754267.1:n.905+23C>T
XR_937066.1:n.928C>T