Canonical Allele Identifier: CA1146079131

Gene: EIF2B3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44978659C= , CM000663.2:g.44978659C=	GRCh38
NC_000001.10:g.45444331C= , CM000663.1:g.45444331C=	GRCh37
NC_000001.9:g.45216918C=	NCBI36
NG_015864.1:g.13031G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360403.7:c.149-199G= MANE Select	ENSP00000353575.2:n.149-199G=
ENST00000360403.6:c.149-199G=	ENSP00000353575.2:n.149-199G=
ENST00000372182.6:n.262-199G=
ENST00000372183.7:c.149-199G=	ENSP00000361257.3:n.149-199G=
ENST00000477953.5:n.252-199G=
ENST00000480675.5:c.149-199G=	ENSP00000485842.1:n.149-199G=
ENST00000487532.5:n.261-199G=
ENST00000497010.1:n.261-199G=
ENST00000620860.4:c.149-199G=	ENSP00000483996.1:n.149-199G=
NM_001166588.2:c.149-199G=	NP_001160060.1:n.149-199G=
NM_001261418.1:c.149-199G=	NP_001248347.1:n.149-199G=
NM_020365.4:c.149-199G=	NP_065098.1:n.149-199G=
XM_011542396.1:c.149-199G=	XP_011540698.1:n.149-199G=
XM_017002745.2:c.149-199G=	XP_016858234.1:n.149-199G=
XM_017002746.1:c.-306-199G=	XP_016858235.1:n.-306-199G=
XM_017002747.1:c.-306-199G=	XP_016858236.1:n.-306-199G=
NM_020365.5:c.149-199G= MANE Select	NP_065098.1:n.149-199G=
NM_001166588.3:c.149-199G=	NP_001160060.1:n.149-199G=
NM_001261418.2:c.149-199G=	NP_001248347.1:n.149-199G=