Canonical Allele Identifier: CA408041377

Gene: IDH3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2664188T>C , CM000682.2:g.2664188T>C	GRCh38
NC_000020.10:g.2644834T>C , CM000682.1:g.2644834T>C	GRCh37
NC_000020.9:g.2592834T>C	NCBI36
NG_012149.1:g.5010A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006899.5:c.1A>G MANE Select	NP_008830.2:p.Met1Val
ENST00000380843.9:c.1A>G MANE Select	ENSP00000370223.4:p.Met1Val
NM_001258384.1:c.1A>G	NP_001245313.1:p.Met1Val
NM_001258384.2:c.1A>G	NP_001245313.1:p.Met1Val
NM_001258384.3:c.1A>G	NP_001245313.1:p.Met1Val
NM_001330763.1:c.1A>G	NP_001317692.1:p.Met1Val
NM_001330763.2:c.1A>G	NP_001317692.1:p.Met1Val
NM_006899.3:c.1A>G	NP_008830.2:p.Met1Val
NM_006899.4:c.1A>G	NP_008830.2:p.Met1Val
NM_174855.2:c.1A>G	NP_777280.1:p.Met1Val
NM_174855.3:c.1A>G	NP_777280.1:p.Met1Val
NM_174855.4:c.1A>G	NP_777280.1:p.Met1Val
NR_136344.1:n.36A>G
NR_136344.2:n.29A>G
ENST00000380843.8:c.1A>G	ENSP00000370223.4:p.Met1Val
ENST00000380851.9:c.1A>G	ENSP00000370232.5:p.Met1Val
ENST00000462967.5:n.28A>G
ENST00000474315.5:c.1A>G	ENSP00000482773.1:p.Met1Val
ENST00000488299.5:n.1A>G
ENST00000491065.1:n.22A>G
ENST00000613370.1:c.1A>G	ENSP00000484922.1:p.Met1Val
XM_005260716.1:c.1A>G	XP_005260773.1:p.Met1Val
XR_001754265.1:n.29A>G
XR_001754266.1:n.29A>G
XR_001754267.1:n.29A>G
XR_937066.1:n.29A>G